JP2020501788A - Surgical stapling system - Google Patents

Abstract

A system is disclosed. The system may include an end effector configured to receive a compatible replaceable staple cartridge, the end effector having a first outer surface, and a classification identification of the end effector on the first outer surface. It is engraved on. The system may also include a compatible replaceable staple cartridge having a second outer surface, with a classification identification of the compatible replaceable staple cartridge imprinted on the second outer surface. The classification identification of a compatible replaceable staple cartridge may correspond to the classification identification of the end effector.

Description

  The present invention relates to surgical instruments and, in various situations, to surgical stapling and cutting instruments and staple cartridges for use therewith, designed for stapling and cutting tissue.

The various features of the embodiments described herein, together with their advantages, can be understood by the following description in conjunction with the accompanying drawings, in which:
FIG. 9 is a perspective view of an embodiment of a replaceable surgical tool assembly operably connected to an embodiment of a handle assembly. FIG. 2 is an exploded view of a portion of the handle assembly and the replaceable surgical tool assembly of FIG. 1. FIG. 3 is a perspective view of the embodiment of the replaceable surgical tool assembly shown in FIGS. 1 and 2 with portions omitted for clarity. FIG. 4 is a perspective view of a proximal portion of the embodiment of the replaceable surgical tool assembly shown in FIGS. 1-3, with some portions omitted for clarity. FIG. 5 is an exploded view of a proximal portion of the replaceable surgical tool assembly of FIGS. FIG. 6 is an exploded view of a distal portion of the replaceable surgical tool assembly of FIGS. FIG. 7 illustrates the use of an embodiment of the replaceable surgical tool assembly to perform a medical procedure known as an inferior anterior resection in the human pelvic region. FIG. 8 is a top view of a portion of the replaceable surgical tool assembly shown in FIG. FIG. 9 is another top view of the replaceable surgical tool assembly shown in FIG. 8, a portion of which is shown in cross-section. FIG. 10 is a partial perspective view of a distal portion of the replaceable surgical tool assembly of FIG. 9; 11 is a cross-sectional view of the replaceable surgical tool assembly of FIG. 10 taken along line 11-11 of FIG. FIG. 14 is a partial perspective view of a portion of another replaceable surgical tool assembly. FIG. 9 is a cross-sectional end view of a shaft assembly portion of another replaceable surgical tool embodiment. FIG. 9 is a cross-sectional end view of a shaft assembly portion of another replaceable surgical tool embodiment. FIG. 4 is a top cross-sectional view of a portion of an embodiment of an exchangeable surgical tool in an articulated configuration. FIG. 9 is a top view of a portion of another surgical end effector and elongated shaft assembly mechanism with the surgical end effector in an unarticulated position (solid line) and in an articulated position (virtual line). FIG. 4 is a perspective view of a portion of an end effector of a replaceable surgical tool using an anvil cap to cover a portion of a firing member parking area within the end effector. FIG. 17 is another perspective view of a portion of the surgical end effector of FIG. 16 with an anvil cap omitted for clarity. FIG. 17 is a side view of the surgical end effector of FIG. 16 with the anvil in an open configuration. FIG. 19 is a cross-sectional side view of the surgical end effector of FIG. 18. FIG. 19 is a cross-sectional side view of the surgical end effector of FIG. 18 during the beginning of the anvil closing process. FIG. 20 is another cross-sectional side view of the surgical end effector of FIGS. 18 and 19 with the anvil in a fully closed position. FIG. 21 is another cross-sectional side view of the surgical end effector of FIG. 20 after the firing member has been advanced distally from the firing member retention area. FIG. 4 is a perspective view of an embodiment of a distal closure member. FIG. 22 is a side view of a portion of a replaceable surgical tool assembly using the distal closure member of FIG. 21 with the anvil of the surgical end effector portion in a fully closed position. FIG. 23 is another side view of a portion of the replaceable surgical tool assembly of FIG. 22 with the distal closure member in an initial open position. FIG. 23 is another side view of a portion of the replaceable surgical tool assembly of FIG. 22 with the distal closure member in another open position. FIG. 23 is another side view of a portion of the replaceable surgical tool assembly of FIG. 22 with the anvil in a fully open position. FIG. 9 is a perspective view of another distal closure member embodiment. FIG. 5 is a side view of another anvil embodiment. FIG. 27 is a partial cross-sectional side view of another replaceable surgical tool assembly using the distal closure member of FIG. 26 and the embodiment of the anvil of FIG. 27 with the anvil in a fully closed position. FIG. 29 is another partial cross-sectional side view of the replaceable surgical tool assembly of FIG. 28 with the anvil in a fully open position. FIG. 9 is a perspective view of another distal closure member embodiment. FIG. 31 is a partial cross-sectional side view of another interchangeable surgical tool assembly using the embodiment of the distal closure member of FIG. 30 with the anvil in a fully open position. FIG. 14 is a partial cross-sectional side view of another interchangeable surgical tool assembly with the anvil in a fully closed position. FIG. 33 is another partial cross-sectional side view of the replaceable surgical tool assembly of FIG. 32 with the anvil in a fully open position. FIG. 14 is a side view of a portion of another replaceable surgical tool assembly with the anvil in a fully closed position. FIG. 35 is another side view of a portion of the replaceable surgical tool assembly of FIG. 34 with the anvil in a fully open position. FIG. 14 is a side view of a portion of another replaceable surgical tool assembly with the anvil in a fully closed position. FIG. 37 is another side view of a portion of the replaceable surgical tool assembly of FIG. 36 with the anvil in a partially open position. FIG. 14 is a side view of a portion of another replaceable surgical tool assembly with the anvil in a fully closed position. FIG. 39 is another side view of a portion of the replaceable surgical tool assembly of FIG. 38 with the anvil in a partially open position. FIG. 4 is a bottom perspective view of an embodiment of a cumming or thread assembly. FIG. 10 is a top view of a portion of an embodiment of a surgical end effector with an unfired surgical staple cartridge loaded therein, the camming assembly in a starting position, and in an unlocked engagement with a firing member locking member. is there. 41. The surgical end of FIG. 41 having an improperly unfired surgical staple cartridge mounted therein, the cumming assembly in the starting position, and the firing member lock in lock engagement with the firing member. FIG. 4 is a top view of a portion of an embodiment of an effector. FIG. 9 is an exploded perspective view of a portion of an anvil, firing member, sled assembly, and firing member lock embodiment of another replaceable surgical tool assembly embodiment. FIG. 44 is a partial cross-sectional view of the distal portion of the replaceable surgical tool assembly of FIG. 43 with the firing member omitted for clarity. With the unfired surgical staple cartridge properly seated in the surgical end effector, the anvil in the open position, and the firing member in the starting position, the distal portion of the replaceable surgical tool assembly of FIG. It is another partial sectional view. FIG. 46 is another partial cross-sectional view of the distal portion of the replaceable surgical tool assembly of FIG. 45 with the anvil in the fully closed position and the firing member in the initial firing position. FIG. 46 is another partial cross-sectional view of the distal portion of the replaceable surgical tool assembly of FIG. 45, with the anvil in the fully closed position and the firing member advanced further distally within the surgical end effector. FIG. 48 is another partial cross-sectional view of the distal portion of the replaceable surgical tool assembly of FIG. 47 with the anvil in the fully closed position and the firing member retracted back to the starting position just before contacting the firing member lock. is there. Another partial cross-section of the distal portion of the replaceable surgical tool assembly of FIG. 48, wherein the anvil is in the fully closed position and the firing member has been retracted back to the starting position after first contacting the firing member lock. FIG. FIG. 50 is another partial cross-sectional view of the distal portion of the replaceable surgical tool assembly of FIG. 49 with the anvil in the fully closed position and the firing member retracted back to the starting position. FIG. 14 is a side cross-sectional view of a portion of another replaceable surgical tool assembly embodiment with an unfired surgical staple cartridge loaded in a surgical end effector and a firing member in a starting position or configuration. FIG. 53 is another cross-sectional side view of the embodiment of the replaceable surgical tool assembly of FIG. 51 after the firing member has begun to advance distally through the surgical end effector. FIG. 53 is another side cross-sectional view of the embodiment of the replaceable surgical tool assembly of FIGS. 51 and 52 while retracting the firing member to a starting position. FIG. 54 is another cross-sectional side view of the embodiment of the replaceable surgical tool assembly of FIGS. 51-53 after the firing member has been further retracted toward the starting position. FIG. 55 is another side cross-sectional view of the embodiment of the replaceable surgical tool assembly of FIGS. 51-54 after the firing member has been fully retracted and returned to the starting position. FIG. 9 is an exploded perspective view of a firing member, a sled assembly, a firing member, and a portion of a firing member locking member of another replaceable surgical tool assembly embodiment. Implementation of the replaceable surgical tool assembly of FIG. 56 with the anvil of the surgical end effector in the open position prior to placing the unfired surgical staple cartridge in the surgical end effector and the firing member in the starting position. It is a side sectional view of a part of form. 58 is another side cross-sectional view of a portion of the embodiment of the replaceable surgical tool assembly of FIG. 57 with the unfired surgical staple cartridge installed in the surgical end effector and the anvil in a closed position. FIG. 59 is a top cross-sectional view of a portion of the embodiment of the replaceable surgical tool assembly of FIG. 58 with the firing member lock in a disengaged configuration with respect to the firing member. FIG. 59 is another side cross-sectional view of a portion of the embodiment of the replaceable surgical tool assembly of FIGS. 58 and 59 after the firing member has first been distally advanced; FIG. 61 is another cross-sectional side view of a portion of the embodiment of the replaceable surgical tool assembly of FIGS. 58-60 while retracting back to a starting position. FIG. 62 is a top view of a portion of the embodiment of the replaceable surgical tool assembly of FIG. 61. Another of the portions of the embodiment of the replaceable surgical tool assembly of FIGS. 58-62 after the firing member has been fully retracted back to the starting position and in lock engagement with the firing member lock. It is a side sectional view. FIG. 14 is an exploded perspective view of a portion of an articulation and articulation lock embodiment of another replaceable surgical tool assembly embodiment. FIG. 66 is a perspective view of an embodiment of a lock spring assembly of the embodiment of the joint lock of FIG. 64. FIG. 65 is a top view of an embodiment of the end effector mounting assembly of the embodiment of the replaceable surgical tool assembly of FIG. 64. 65 is a top view of a portion of the embodiment of the replaceable surgical tool assembly of FIG. 64 with the surgical end effector in a non-articulated configuration. FIG. 67 is another top view of a portion of the embodiment of the replaceable surgical tool assembly of FIG. 67 during initial application of articulation to the articulation; FIG. 69 is a bottom view of a portion of the embodiment of the replaceable surgical tool assembly of FIG. 68. FIG. 69 is another bottom view of a portion of the embodiment of the replaceable surgical tool assembly of FIG. 69 with the surgical end effector in an articulated configuration. FIG. 14 is an exploded perspective view of a portion of an articulation and articulation lock embodiment of another replaceable surgical tool assembly embodiment. FIG. 72 is a top view of an embodiment of the end effector mounting assembly of the embodiment of the replaceable surgical tool assembly of FIG. 71. FIG. 72 is a top view of a portion of the embodiment of the replaceable surgical tool assembly of FIG. 71 with the surgical end effector in a non-articulated configuration. FIG. 74 is a partial cross-sectional view of a portion of the embodiment of the joint lock of FIG. 73, taken along line 74-74 of FIG. 73; FIG. 74 is another top view of a portion of the embodiment of the replaceable surgical tool assembly of FIG. 73 during an initial application of articulation to the articulation. FIG. 76 is another top view of a portion of the embodiment of the replaceable surgical tool assembly of FIG. 75 with the surgical end effector in an articulated configuration and the articulation lock in an unlocked configuration. FIG. 76 is another top view of a portion of the embodiment of the replaceable surgical tool assembly of FIG. 75 with the surgical end effector in the articulated configuration and the articulation lock in the locked configuration. FIG. 14 is an exploded perspective view of a portion of an articulation and articulation lock embodiment of another replaceable surgical tool assembly embodiment. FIG. 79 is a top view of a portion of the embodiment of the replaceable surgical tool assembly of FIG. 78 with the surgical end effector in an un-articulated configuration. FIG. 80 is a side cross-sectional view of a portion of the replaceable surgical tool assembly of FIG. 79 taken along line 80-80 of FIG. 79. FIG. 81 is another cross-sectional view of a portion of the interchangeable surgical tool assembly of FIG. 80 during initial application of articulation to the articulation lock. FIG. 83 is another side cross-sectional view of a portion of the interchangeable surgical tool assembly of FIG. 81 with the articulation locked in place by an articulation lock. FIG. 14 is an exploded perspective view of a portion of a spine assembly, articulation, and articulation lock embodiment of another replaceable surgical tool assembly embodiment. FIG. 84 is a top view of the distal end of the spine assembly and a portion of the joint locking mechanism of the embodiment of the replaceable surgical tool assembly of FIG. 83. FIG. 14 is an exploded perspective view of a portion of a spine assembly, articulation, and articulation lock embodiment of another replaceable surgical tool assembly embodiment. FIG. 86 is another exploded perspective view of a spine assembly and a portion of a joint joint and a joint lock of the replaceable surgical tool assembly of FIG. 85. FIG. 86 is a top cross-sectional view of the replaceable surgical tool assembly of FIG. 85 with the surgical end effector in an un-articulated configuration. FIG. 88 is another top cross-sectional view of the replaceable surgical tool assembly of FIG. 87 with the surgical end effector in an articulated configuration and the articulation lock unlocked. FIG. 89 is another top cross-sectional view of the replaceable surgical tool assembly of FIG. 88 with the surgical end effector in the articulated configuration and the articulation lock in the locked configuration. FIG. 14 is an exploded perspective view of a portion of a spine assembly, articulation, and articulation lock embodiment of another replaceable surgical tool assembly embodiment. FIG. 91 is a top cross-sectional view of the replaceable surgical tool assembly of FIG. 90 with the surgical end effector in a non-articulated configuration; FIG. 92 is another top cross-sectional view of the replaceable surgical tool assembly of FIG. 91 with the surgical end effector in an articulated configuration and the articulation lock in an unlocked configuration. 93 is a partial cross-sectional view of the joint lock of FIG. 92 taken along line 93-93 of FIG. 92. FIG. 92 is another top cross-sectional view of the replaceable surgical tool assembly of FIG. 91 with the surgical end effector in an articulated configuration and the articulation lock in a locked configuration. FIG. 95 is a partial cross-sectional view of the joint lock of FIG. 94 taken along line 95-95 of FIG. 94. FIG. 3 is a perspective view of a portion of an embodiment of an articulation stroke amplifier. 97 is a cross-sectional end view of a shaft assembly of an embodiment of a replaceable surgical tool assembly having the articulation stroke amplifier of FIG. 96 therein. 97 is a top view of a portion of the embodiment of the articulation stroke amplifier of FIG. 96 in a non-actuated configuration. FIG. 98B is another top view of a portion of the articulation stroke amplifier of FIG. 98A after axial articulation has been applied in a first axial direction. FIG. 98B is another top view of a portion of the articulation stroke amplifier of FIG. 98A after another axial articulation has been applied in a second axial direction. FIG. 9 is a top cross-sectional view of a portion of a shaft assembly of an embodiment of a replaceable surgical tool assembly including another embodiment of an articulation stroke amplifier in a non-actuated configuration. FIG. 99B is another top cross-sectional view of the shaft assembly and articulation stroke amplifier of FIG. 99A after axial articulation in a first axial direction has been applied. FIG. 14 is a top cross-sectional view of a portion of a shaft assembly of another replaceable surgical tool assembly embodiment, including another articulation stroke amplifier embodiment in a non-actuated configuration. FIG. 99C is another top cross-sectional view of the shaft assembly and articulation stroke amplifier of FIG. 99C after axial articulation in a first axial direction has been applied. FIG. 3 is an exploded perspective view of a channel and a staple cartridge. FIG. 110 is an elevation view of the channel and staple cartridge of FIG. 100. FIG. 112 is a cross-sectional elevation view of the channel and staple cartridge of FIG. 100, taken across the plane shown in FIG. 101; FIG. 3 is an exploded perspective view of a channel and a staple cartridge. FIG. 104 is an elevation view of the staple cartridge of FIG. 103. FIG. 104 is a cross-sectional elevation view of the channel and staple cartridge of FIG. 103, taken across the plane shown in FIG. 104; FIG. 4 is an exploded elevation view of a channel and a staple cartridge. FIG. 107 is an elevational view of the channel and staple cartridge of FIG. 106, showing the staple cartridge installed completely within the channel; FIG. 4 is an exploded elevation view of a channel and a staple cartridge. FIG. 109 is an elevational view of the channel and staple cartridge of FIG. 108, showing the staple cartridge completely installed in the channel; FIG. 109 is an elevational view of the staple cartridge of FIG. 106 and the channel of FIG. 108, showing the staple cartridge partially installed in the channel; FIG. 3 is a perspective view of a part of the staple cartridge. FIG. 3 is a perspective view of a part of the staple cartridge. It is a perspective view of an end effector. Figure 4 shows a table of identification of various types of end effectors. Figure 4 shows a table of identification of various types of end effectors.

  Corresponding reference characters indicate corresponding parts throughout the drawings. The exemplifications set forth herein illustrate, in one form, various embodiments of the invention, and such exemplifications are not to be construed as limiting the scope of the invention in any manner. Absent.

The applicant of the present application owns the following U.S. patent applications filed on December 21, 2016, each of which is incorporated herein by reference in its entirety:
-U.S. Patent Application No. 15 / 386,185, entitled "SURGICAL STAPLING INSTRUMENTS AND REPLACEABLE TOOL ASSEMBLEES THEREOF",
-U.S. Patent Application No. 15 / 386,221 entitled "LOCKOUT ARRANGEMENTS FOR SURGICAL END EFFECTORS";
-U.S. Patent Application No. 15 / 386,209, entitled "SURGICAL END EFFECTORS AND FIRING MEMBERS THEREOF",
-U.S. Patent Application No. 15 / 386,198, Title of Invention "LOCKOUT ARRANGEMENTS FOR SURGICAL END EFFECTORS AND REPLACEABLE TOOL ASSEMBLIES", and-U.S. Patent Application No. 15 / 386,240, Title of Invention "SUDARDEFFALED AGREED ECE FIRING MEMBERS THEREFOR ”.

The applicant of the present application owns the following U.S. patent applications filed on December 21, 2016, each of which is incorporated herein by reference in its entirety:
-U.S. Patent Application No. 15 / 385,939, entitled "STAPLE CARTRIDGES AND ARRANGEMENTS OF STAPLES AND STAPLE CAVITIES THEREIN",
-U.S. Patent Application No. 15 / 385,941, entitled "SURGICAL TOOL ASSEMBLIES WITH CLUTCHING ARRANGEMENTS FOR SHIFTING BETWEEN CLOSURE WORKS STORE RESOURCE STORE RESOURCE STORE RESOURCE STORE PRODUCT SERIES RESOURCES
-U.S. Patent Application No. 15 / 385,943, entitled "SURGICAL STAPLING INSTRUMENTS AND STAPLE-FORMING ANVILS",
-U.S. Patent Application No. 15 / 385,950, entitled "SURGICAL TOOL ASSEMBLIES WITH CLOSE STROKE REDUCTION FEATURES",
-U.S. Patent Application No. 15 / 385,945, entitled "STAPLE CARTRIDGES AND ARRANGEMENTS OF STAPLES AND STAPLE CAVITIES THEREIN",
-U.S. Patent Application No. 15 / 385,946, entitled "SURGICAL STAPLING INSTRUMENTS AND STAPLE-FORMING ANVILS",
-U.S. Patent Application No. 15 / 385,951, entitled "SURGICAL INSTRUMENTS WITH JAW OPENING FEATURES FOR INCREASING A JAW OPENING DISTANCE,"
-U.S. Patent Application No. 15 / 385,953, entitled "METHODS OF STAPLING TISSUE",
-U.S. Patent Application No. 15 / 385,954, entitled "FIRING MEMBERS WITH NON-PARALLEL JAW ENGAGENENT FEATURES FOR SURGICAL END EFFECTORS",
-U.S. Patent Application No. 15 / 385,955, entitled "SURGICAL END EFFECTORS WITH EXPANDABLE TISSUE STOP ARRANGEMENTS",
-U.S. Patent Application No. 15 / 385,948, entitled "SURGICAL STAPLING INSTRUMENTS AND STAPLE-FORMING ANVILS",
-U.S. Patent Application No. 15 / 385,956, entitled "SURGICAL INSTRUMENTS WITH POSITIVE JAW OPENING FEATURES",
-U.S. Patent Application No. 15 / 385,958, entitled "SURGICAL INSTRUMENTS WITH LOCKOUT ARRANGEMENTS FOR PREVENTING FIRING SYSTEM ACTUATION UNLESS AN UNSPENT STAPLET REPORT, U.S. Pat. The name "STAPLE CARTRIDGES AND ARRANGEMENTS OF STAPLES AND STAPLE CAVITIES THEREIN".

The applicant of the present application owns the following U.S. patent applications filed on December 21, 2016, each of which is incorporated herein by reference in its entirety:
-U.S. Patent Application No. 15 / 385,896, entitled "METHOD FOR RESETTING A FUSE OF A SURGICAL INSTRUMENT SHAFT",
-U.S. Patent Application No. 15 / 385,898, entitled "STAPLE FORMING POCKET ARRANGEMENT TO ACCOMMODATE DIFFERENT TYPES OF STAPLES",
-U.S. Patent Application No. 15 / 385,899, entitled "SURGICAL INSTRUMENT COMPRISING IMPROVED JAW CONTROL",
-U.S. Patent Application No. 15 / 385,901, entitled "STAPLE CARTRIDGE AND STAPLE CARTRIDGE CHANNEL COMPRISING WINDOWS DEFINED THEREIN",
-U.S. Patent Application No. 15 / 385,902, entitled "SURGICAL INSTRUMENT COMPRISING A CUTTING MEMBER",
-US Patent Application No. 15 / 385,904, entitled "STAPLE FIRING MEMBER COMPRISING A MISSING CARTRIDGE AND / OR SPENT CARTRIDGE LOCKOUT",
-U.S. Patent Application No. 15 / 385,905, entitled "FIRING ASSEMBLY COMPRISING A LOCKOUT",
-U.S. Patent Application No. 15 / 385,907, entitled "SURGICAL INSTRUMENT SYSTEM COMPRISING AN END EFFECTOR LOCKOUT AND A FIRING ASSEMBLY LOCKOUT",
-U.S. Patent Application No. 15 / 385,908, Title of Invention "FIRING ASSEMBLY COMPRISING A FUSE"; .

The applicant of the present application owns the following U.S. patent applications filed on December 21, 2016, each of which is incorporated herein by reference in its entirety:
-U.S. Patent Application No. 15 / 385,920, entitled "STAPLE FORMING POCKET ARRANGEMENTS",
-U.S. Patent Application No. 15 / 385,913, entitled "ANVIL ARRANGEMENTS FOR SURGICAL STAPLERS",
-U.S. Patent Application No. 15 / 385,914, entitled "METHOD OF DEFORMING STAPLES FROM TWO DIFFERENT TYPES OF STAPLE CARTRIDGES WITH THE THE SAME SURGICAL STAPLING INSTRUMENT,"
-U.S. Patent Application No. 15 / 385,893, entitled "BILATERALLY ASYMMETRIC STAPLE FORMING POCKET PAIRS",
-U.S. Patent Application No. 15 / 385,929, entitled "CLOSURE MEMBERS WITH CAM SURFACE ARRANGEMENTS FOR SURGICAL INSTRUMENTS WITH SEPARATE AND DISTINCT CLOSURE AND FIRINGS,"
-U.S. Patent Application No. 15 / 385,911, entitled "SURGICAL STAPLERS WITH INDEPENDENTLY ACTUATABLE CLOING AND FIRING SYSTEMS",
-U.S. Patent Application No. 15 / 385,927, entitled "SURGICAL STAPLING INSTRUMENTS WITH SMART STAPLE CARTRIDGES",
-U.S. Patent Application No. 15 / 385,917, entitled "STAPLE CARTRIDGE COMPRISING STAPLES WITH DIFFERENT CLAMPING BREADTHS",
-U.S. Patent Application No. 15 / 385,900, entitled "STAPLE FORMING POCKET ARRANGEMENTS COMPRISING PRIMARY SIDEWALLS AND POCKET SIDEWALLS",
U.S. Patent Application No. 15 / 385,931, entitled "NO-CARTRIDGE AND SPENT CARTRIDGE LOCKOUT ARRANGEMENTS FOR SURGICAL STAPLERS",
-U.S. Patent Application No. 15 / 385,915, entitled "FIRING MEMBER PIN ANGLE",
-U.S. Patent Application No. 15 / 385,897, entitled "STAPLE FORMING POCKET ARRANGEMENTS COMPRISING ZONED FORMING SURFACE GROOVES",
-U.S. Patent Application No. 15 / 385,922, entitled "SURGICAL INSTRUMENT WITH MULTIPLE FAILURE RESPONSE MODES,"
-U.S. Patent Application No. 15 / 385,924, entitled "SURGICAL INSTRUMENT WITH PRIMARY AND SAFETY PROCESSORS",
-U.S. Patent Application No. 15 / 385,912, entitled "SURGICAL INSTRUMENTS WITH JAWS THAT ARE PIVOTABLE ABOUT A FIXED AXIS AND INCLUDED SEPARATE AND DISTINCE CROSURENED CLOSURE ANS REGISTERS
-U.S. Patent Application No. 15 / 385,910, entitled "ANVIL HAVING A KNIFE SLOT WIDTH",
-U.S. Patent Application No. 15 / 385,903, title of invention "CLOSURE MEMBER ARRANGEMENTS FOR SURGICAL INSTRUMENTS", and-U.S. Patent Application No. 15 / 385,906, title of invention "FIRING MEMBER PIN CONFIGURATIONS".

The applicant of the present application owns the following U.S. patent applications filed on December 21, 2016, each of which is incorporated herein by reference in its entirety:
-U.S. Patent Application No. 15 / 386,188, entitled "STEPTED STAPLE CARTRIDGE WITH ASYMMETRIC STAPLES",
-U.S. Patent Application No. 15 / 386,192, entitled "STEPTED STAPLE CARTRIDGE WITH TISSUE RETENTION AND GAP SETTING FEATURES",
-U.S. Patent Application No. 15,386,206, entitled "STAPLE CARTRIDGE WITH DEFORMABLE DRIVER RETENTION FEATURES",
-U.S. Patent Application No. 15 / 386,226, entitled "DURABILITY FEATURES FOR END EFFECTORS AND FIRING ASSEMBLIES OF SURGICAL STAPLING INSTRUMENTS",
-U.S. Patent Application No. 15 / 386,222, Title of the Invention "SURGICAL STAPLING INSTRUMENTS HAVING END EFFECTORS WITH POSITIVE OPENING FEATURES", and-U.S. Patent Application No. 15 / 386,236, Title of the Invention "CONNECTION CONNECTIONS UNITS FOR SURGICAL STAPLING INSTRUMENTS ".

The applicant of the present application owns the following U.S. patent applications filed on December 21, 2016, each of which is incorporated herein by reference in its entirety:
-U.S. Patent Application No. 15 / 385,887, entitled "METHOD FOR ATTACHING A SHAFT ASSEMBLY TO A SURGICAL INSTRUMENT AND, ALTERNATIVELY, TO A SURGICAL ROBOT",
-U.S. Patent Application No. 15 / 385,889, entitled "SHAFT ASSEMBLY COMPRISING A MANUALLY-OPERABLE RETRACTION SYSTEM FOR US WITH A MOTORIZED SURGITAL INSTRUMENTS,"
-U.S. Patent Application No. 15 / 385,890, entitled "SHAFT ASSEMBLY COMPRISING SEPARATELY ACTUATABLE AND RETRACTABLE SYSTEMS",
-U.S. Patent Application No. 15 / 385,891, entitled "SHAFT ASSEMBLY COMPRISING A CLUTCH CONFIGURED TO ADAPT THE OUTPUT OF A ROTARY FIRING MEMBER TO TWO DIFFERENTS,"
-U.S. Patent Application No. 15 / 385,892, entitled "SURGICAL SYSTEM COMPRISING A FIRING MEMBER ROTATABLE INTO AN ARTICULATION STATE TOTO ARTICULATE AN END EFFECTOR FURTHER FO
U.S. Patent Application No. 15 / 385,894, Title of the Invention "SHAFT ASSEMBLY COMPRISING A LOCKOUT";

The applicant of the present application owns the following U.S. patent applications filed on December 21, 2016, each of which is incorporated herein by reference in its entirety:
-U.S. Patent Application No. 15 / 385,916, entitled "SURGICAL STAPLING SYSTEMS,"
-U.S. Patent Application No. 15 / 385,918, entitled "SURGICAL STAPLING SYSTEMS",
-U.S. Patent Application No. 15 / 385,919, entitled "SURGICAL STAPLING SYSTEMS",
-U.S. Patent Application No. 15 / 385,921, entitled "SURGICAL STAPLE CARTRIDGE WITH MOVABLE CAMMING MEMBER CONFIGURATION TO DISENGAGE FIRING MEMBER LOCKOUT FEATURES,"
-U.S. Patent Application No. 15 / 385,925, entitled "JAW ACTUATED LOCK ARRANGEMENTS FOR PREVENTING ADVANCEMENT OF A FIRING MEMBER IN A SURGERIAL END ENGINE SERIAL ENGINE REFERENCE SIGNAL ENGINE INTERNATIONAL SERIES
-U.S. Patent Application No. 15 / 385,926, entitled "AXIALLY MOVABLE CLOSURE SYSTEM ARRANGEMENTS FOR APPLYING CLOSURE MOTIONS TO JAWS OF OF SURGICAL INSTRUMENTS",
-U.S. patent application Ser. No. 15 / 385,928, entitled "PROTECTIVE COVER ARRANGEMENTS FOR A JOINT INTERFACE BETWEEN A MOVABLE JAW AND ACTUAL SHAFT OF ASURGAIN INSTRUMENT,"
-U.S. Patent Application No. 15 / 385,930, entitled "SURGICAL END EFFECTOR WITH TWO SEPARATE COOPERATING OPENING FEATURES FOR OPENING AND CLOSING END EFFECTOR JAWS";
-U.S. Patent Application No. 15 / 385,932, entitled "ARTICULABLE SURGICAL END EFFECTOR WITH ASYMMETRIC SHAFT ARRANGEMENT",
-U.S. Patent Application No. 15 / 385,933, entitled "ARTICULABLE SURGICAL INSTRUMENT WITH INDEPENDENT PIVOTABLE LINKAGE DISTAL OF AN ARTICULATION LOCK",
-U.S. Patent Application No. 15 / 385,934, entitled "ARTICULATION LOCK ARRANGEMENTS FOR LOCKING AN END EFFECTOR IN AN ARTICULATED POSITION IN RESPONSE TO ACTUS ACTION WORKS AREA FUSION AREA FUSION AREA
U.S. Patent Application No. 15 / 385,935, title of invention "LATEALLY ACTUATABLE ARTICULATION LOCK ARRANGEMENTS FOR LOCKING AN END EFFECTOR OF A SURGITAL INSTRUMENT IN AUTHORUS, US Pat. "ARTICULABLE SURGICAL INSTRUMENTS WITH ARTICULATION STROKE AMPLIFICATION FEATURES".

The applicant of the present application owns the following U.S. patent applications filed on June 24, 2016, the entire contents of each of which are incorporated herein by reference:
-U.S. Patent Application No. 15 / 191,775, entitled "STAPLE CARTRIDGE COMPRISING WIRE STAPLES AND STAMPED STAPLES",
-U.S. Patent Application No. 15 / 191,807, entitled "STAPLING SYSTEM FOR USE WITH WIRE STAPLES AND STAMPED STAPLES",
-U.S. Patent Application No. 15 / 191,834, entitled "STAMPED STAPLES AND STAPLE CARTRIDGES USING THE SAME",
U.S. Patent Application No. 15 / 191,788, Title of Invention "STAPLE CARTRIDGE COMPRISING OVERDRIVEN STAPLES";

The applicant of the present application owns the following U.S. patent applications filed on June 24, 2016, the entire contents of each of which are incorporated herein by reference:
-U.S. Design Patent Application No. 29 / 569,218, entitled "SURGICAL FASTENER",
-U.S. Design Patent Application No. 29 / 569,227, entitled "SURGICAL FASTENER",
-U.S. Design Patent Application No. 29 / 569,259, title of the invention "SURGICAL FASTENER CARTRIDGE", and-U.S. Design Patent Application No. 29 / 569,264, title of the invention "SURGICAL FASTENER CARTRIDGE".

The applicant of the present application owns the following patent applications filed on April 1, 2016, each of which is incorporated herein by reference in its entirety:
-U.S. Patent Application No. 15 / 089,325, entitled "METHOD FOR OPERATING A SURGICAL STAPLING SYSTEM",
-U.S. Patent Application No. 15 / 089,321, entitled "MODULAR SURGICAL STAPLING SYSTEM COMPRISING A DISPLAY",
-U.S. Patent Application No. 15 / 089,326, entitled "SURGICAL STAPLING SYSTEM COMPRISING A DISPLAY INCLUDING A RE-ORIENTABLE DISPLAY FIELD",
-U.S. Patent Application No. 15 / 089,263, entitled "SURGICAL INSTRUMENT HANDLE ASSEMBLY WITH RECONFIGURE GRIP PORTION,"
-U.S. Patent Application No. 15 / 089,262, entitled "ROTARY POWERED SURGICAL INSTRUMENT WITH MANUALLY ACTUABLE BAILOUT SYSTEM",
-U.S. Patent Application No. 15 / 089,277, entitled "SURGICAL CUTTING AND STAPLING END EFFECTOR WITH ANVIL CONCENTRIC DRIVE MEMBER",
-U.S. Patent Application No. 15 / 089,296, entitled "INTERCHANGEABLE SURGICAL TOOL ASSEMBLY WITH A SURGICAL END EFFECTOR THAT IS SELECTIVELY ROTATABLE ABOUT ASH FASH
-U.S. Patent Application No. 15 / 089,258, entitled "SURGICAL STAPLING SYSTEM COMPRISING A SHIFTABLE TRANSMISSION",
-U.S. Patent Application No. 15 / 089,278, entitled "SURGICAL STAPLING SYSTEM CONFIGURATION TO PROVIDE SELECTIVE CUTTING OF TISSUE",
-U.S. Patent Application No. 15 / 089,284, entitled "SURGICAL STAPLING SYSTEM COMPRISING A CONTOURABLE SHAFT",
-U.S. Patent Application No. 15 / 089,295, entitled "SURGICAL STAPLING SYSTEM COMPRISING A TISSUE COMPRESSION LOCKOUT",
-U.S. Patent Application No. 15 / 089,300, entitled "SURGICAL STAPLING SYSTEM COMPRISING AN UNCLAMPING LOCKOUT",
-U.S. Patent Application No. 15 / 089,196, entitled "SURGICAL STAPLING SYSTEM COMPRISING A JAW CLOSURE LOCKOUT",
-U.S. Patent Application No. 15 / 089,203, entitled "SURGICAL STAPLING SYSTEM COMPRISING A JAW ATTACHMENT LOCKOUT",
-U.S. Patent Application No. 15 / 089,210, entitled "SURGICAL STAPLING SYSTEM COMPRISING A SPENT CARTRIDGE LOCKOUT",
-U.S. Patent Application No. 15 / 089,324, entitled "SURGICAL INSTRUMENT COMPRISING A SHIFTING MECHANISM",
-U.S. Patent Application No. 15 / 089,335, entitled "SURGICAL STAPLING INSTRUMENT COMPULSING MULTIPLE LOCKOUTS",
-U.S. Patent Application No. 15 / 089,339, entitled "SURGICAL STAPLING INSTRUMENT",
-U.S. Patent Application No. 15 / 089,253, entitled "SURGICAL STAPLING SYSTEM CONFIGURATION TO APPLY ANNULAR ROWS OF STAPLES HAVING DIFFERENT HEIGHTS",
-U.S. Patent Application No. 15 / 089,304, entitled "SURGICAL STAPLING SYSTEM COMPRISING A GROOVED FORMING POCKET",
-U.S. Patent Application No. 15 / 089,331, entitled "ANVIL MODIFICATION MEMBERS FOR SURGICAL STAPLERS",
-U.S. Patent Application No. 15 / 089,336, entitled "STAPLE CARTRIDGES WITH ATRAUMATIC FEATURES,"
-U.S. Patent Application No. 15 / 089,312, entitled "CIRCULAR STAPLING SYSTEM COMPRISING AN INCISABLE TISSUE SUPPORT",
-U.S. Patent Application No. 15 / 089,309, title of invention "CIRCULAR STAPLING SYSTEM COMPRISING ROTARY FIRING SYSTEM", and-U.S. Patent Application No. 15 / 089,349, title of invention "CIRCULAR STAPLING SYSTEM CONFIGURATION COLOR CONFIGURATION CONFIGURATION CONFIGURATION.

Applicants also own a U.S. patent application filed December 31, 2015, identified below, the entire contents of which are each incorporated herein by reference:
-U.S. Patent Application No. 14 / 984,488, entitled "MECHANISMS FOR COMPENSATION FOR BATTERY PACK FAILURE IN POWERED SURGICAL INSTRUMENTS",
-U.S. patent application Ser. No. 14 / 984,525, title of invention "MECHANISMS FOR COMPENSATION FOR DRIVETTRAIN FAILURE IN POWERED SURGICAL INSTRUMENTS", and-U.S. patent application Ser. AND MOTOR CONTROL CIRCUITS ".

Applicants also own a U.S. patent application filed February 9, 2016, identified below, the entire contents of which are each incorporated herein by reference:
-U.S. Patent Application No. 15 / 019,220, entitled "SURGICAL INSTRUMENT WITH ARTICULATING AND AXIALLY TRANSLATABLE END EFFECTOR",
-U.S. Patent Application No. 15 / 019,228, entitled "SURGICAL INSTRUMENTS WITH MULTIPLE LINK ARTICULATION ARRANGEMENTS",
-U.S. Patent Application No. 15 / 019,196, entitled "SURGICAL INSTRUMENT ARTICULATION MECHANISM WITH SLOTTED SECONDARY CONSTRAIN",
-U.S. Patent Application No. 15 / 019,206, entitled "SURGICAL INSTRUMENTS WITH AN END EFFECTOR THAT IS HIGHLY ARTICULATEABLE RELATIVE TO AN ELONGATE SHAFT ASSEMBLY";
-U.S. Patent Application No. 15 / 019,215, entitled "SURGICAL INSTRUMENTS WITH NON-SYMMETRICAL ARTICULATION ARRANGEMENTS",
-U.S. Patent Application No. 15 / 019,227, entitled "ARTICULABLE SURGICAL INSTRUMENTS WITH SINGLE ARTICULATION LINK ARRANGEMENTS",
-U.S. Patent Application No. 15 / 019,235, entitled "SURGICAL INSTRUMENTS WITH TENSIONING ARRANGEMENTS FOR CABLE DRIVEN ARTICULATION SYSTEMS,"
-U.S. Patent Application No. 15 / 019,230; Title of Invention "ARTICULABLE SURGICAL INSTRUMENTS WITH OFF-AXIS FIRING BEAM ARRANGEMENTS"; REDUCTION ARRANGEMENTS ”.

The applicant of the present application also owns U.S. patent applications filed February 12, 2016, identified below, the entire contents of which are each incorporated herein by reference:
-U.S. Patent Application No. 15 / 043,254, entitled "MECHANISMS FOR COMPENSATING FOR DRIVETRAIN FAILURE IN POWERED SURGICAL INSTRUMENTS",
-U.S. Patent Application No. 15 / 043,259, title of invention "MECHANISMS FOR COMPENSATE FOR DIVIVTRAIN FAILURE IN POWERED SURGICAL INSTRUMENTS",
-U.S. Patent Application No. 15 / 043,275; Title of Invention "MECHANISMS FOR COMPENSATE FOR DIVIVTRAIN FAILURE IN POWERED SURGICAL INSTRUMENTS"; and-U.S. Patent Application No. 15 / 043,289; FAILURE IN POWERED SURGICAL INSTRUMENTS ".

The applicant of the present application owns the following patent applications filed on June 18, 2015, the entire contents of which are each incorporated herein by reference:
-U.S. patent application Ser. No. 14 / 742,925, entitled "SURGICAL END EFFECTORS WITH POSITIVE JAW OPENING ARRANGEMENTS",
-U.S. Patent Application No. 14 / 742,941, entitled "SURGICAL END EFFECTORS WITH DUAL CAM ACTUATED JAW CLOSING FEATURES",
-U.S. Patent Application No. 14 / 742,914, entitled "MOVABLE FIRING BEAM SUPPORT ARRANGEMENTS FOR ARTICULATABLE SURGICAL INSTRUMENTS",
-U.S. patent application Ser. No. 14 / 742,900, entitled "ARTICULABLE SURGICAL INSTRUMENTS WITH COMPOSITE FIRING BEAM STRUCTURES WITH CENTER FIRING SUPPORT PORTER PORTER PORTER ART OVER PORT INTERNATIONAL
-U.S. Patent Application No. 14 / 742,885; Title of Invention "DUAL ARTICULATION DRIVE SYSTEM ARRANGEMENTS FOR ARTICULATEABLE SURGICAL INSTRUMENTS"; and-U.S. Patent Application No. 14 / 742,876; SURGICAL INSTRUMENTS ”.

The applicant of the present application owns the following patent applications filed on March 6, 2015, each of which is hereby incorporated by reference in its entirety:
-U.S. Patent Application No. 14 / 640,746, entitled "POWERED SURGICAL INSTRUMENT", currently US Patent Application Publication No. 2016/0256184,
-U.S. Patent Application No. 14 / 640,795, entitled "MULTIPLE LEVEL THRESHOLDS TO MODIFY OPERATION OF POWERED SURGICAL INSTRUMENTS", currently U.S. Patent Application Publication No. 2016/02561185,
-U.S. Patent Application No. 14 / 640,832, entitled "ADAPTIVE TISSUE COMPRESSION TECHNIQUES TO ADJUST CLOSURE RATES FOR MULTIPLE TISSUE TYPES", now U.S. Patent Application Publication No. 2016/0256154.
-U.S. Patent Application No. 14 / 640,935, entitled "OVERLAID MULTI SENSOR RADIO FREQUENCY (RF) ELECTRODE SYSTEM TO MEASURE TISSUE COMPRESSION", now U.S. Patent Application Publication No. 2016/0256071.
-U.S. Patent Application No. 14 / 640,831, entitled "MONITORING SPEED CONTROL AND PRECISION INCREMENTING OF MOTOR FOR POWERED SURGICAL INSTRUMENTS", now U.S. Patent Application Publication No. 2016/0256153;
-U.S. Patent Application No. 14 / 640,859, Title of Invention "TIME DEPENDENT EVALUATION OF SENSOR DATA TO DETERMINE STABILITY, CREEP, AND VISCOELASTIC ELEMENTS OF MEASURES, currently published in U.S. Pat.
-U.S. Patent Application No. 14 / 640,817, entitled "INTERACTIVE FEEDBACK SYSTEM FOR POWERED SURGICAL INSTRUMENTS", currently U.S. Patent Application Publication No. 2016/0256186,
-U.S. Patent Application No. 14 / 640,844, entitled "CONTROL TECHNIQUES AND SUB-PROCESSOR CONTAINED WITHIN MODULAR SHAFT WITH SELECT SELECT CONTROL CONTROL FROM FROM HAND02, U.S. Pat.
-U.S. Patent Application No. 14 / 640,837, entitled "SMART SENSORS WITH LOCAL SIGNAL PROCESSING", currently U.S. Patent Application Publication No. 2016/0256163,
-U.S. Patent Application No. 14 / 640,765, entitled "SYSTEM FOR DETECTION THE THE MIS-INSERTION OF A STAPLE CARTRIDGE INTO A SURGICAL STAPLLER", currently U.S. Patent Application Publication No. 2016/0256160,
-U.S. Patent Application No. 14 / 640,799, entitled "SIGNAL AND POWER COMMUNICATION SYSTEM POSITIONED ON A ROTATABLE SHAFT", currently U.S. Patent Application Publication No. 2016/0256162, and-U.S. Patent Application No. 14/640, No. 780, entitled "SURGICAL INSTRUMENT COMPRISING A LOCKABLE BATTERY HOUSING", currently US Patent Application Publication No. 2016/0256161.

The applicant of the present application owns the following patent applications filed on February 27, 2015, the entire contents of which are each incorporated herein by reference:
-U.S. Patent Application No. 14 / 633,576, entitled "SURGICAL INSTRUMENT SYSTEM COMPRISING AN INSPECTION STATION", currently U.S. Patent Application Publication No. 2016/0249919;
-U.S. patent application Ser. No. 14 / 633,546, entitled "SURGICAL APPARATUS CONFIGURATION TO ASSESS WHEETHER A PERFORMANCE PARAMETER OF THE SURGICAL APPARATUS IS WANTIN ACCESSORIES ANNUAL ACCESSORIES ANNUAL ACCESSORIES ANNUAL ACCESSORIES ANNUAL ACCESSORY
-U.S. Patent Application No. 14 / 633,560, entitled "Surgical Charging Systems THAT Charges And / Or Conditions One Or More Bateries", currently U.S. Patent Application Publication No. 2016/0249910;
-U.S. Patent Application No. 14 / 633,566, entitled "CHARGING SYSTEM THAT ENABLES EMERGENCY RESOLUTIONS FOR CHARGING A BATTERY", currently U.S. Patent Application Publication No. 2016/0249918;
-U.S. Patent Application No. 14 / 633,555, entitled "SYSTEM FOR MONITORING WHEETHER A SURGICAL INSTRUMENT NEEDS TO BE SERVICED", currently U.S. Patent Application Publication No. 2016/0249916;
-U.S. Patent Application No. 14 / 633,542, entitled "REINFORCED BATTERY FOR A SURGICAL INSTRUMENT", currently U.S. Patent Application Publication No. 2016/0249908,
-U.S. Patent Application No. 14 / 633,548, entitled "POWER ADAPTER FOR A SURGICAL INSTRUMENT", currently U.S. Patent Application Publication No. 2016/0249909;
-U.S. Patent Application No. 14 / 633,526, entitled "ADAPTABLE SURGICAL INSTRUMENT HANDLE", currently U.S. Patent Application Publication No. 2016/0249945,
-U.S. Patent Application No. 14 / 633,541, title of invention "MODULAR STAPLING ASSEMBLY", currently U.S. Patent Application Publication No. 2016/0249927, and-U.S. Patent Application No. 14 / 633,562, title of invention. SURGICAL APPARATUS CONFIGURATION TO TRACK AN END-OF-LIFE PARAMETER ", currently U.S. Patent Application Publication No. 2016/0249917.

The applicant of the present application owns the following patent applications filed on December 18, 2014, each of which is hereby incorporated by reference in its entirety:
-U.S. Patent Application No. 14 / 574,478, entitled "SURGICAL INSTRUMENT SYSTEMS COMPRISING AN ARTICULATABLE END EFFECTOR AND MEANS FOR ADJUSTING THE FIRING STORY MERGE FRONT GIRL OF THE GIRL OF THE GIRL OF THE GIRL OF THE FIRING GOVERNING OF THE FIRGING OF THE GIRL
-U.S. Patent Application No. 14 / 574,483, entitled "SURGICAL INSTRUMENT ASSEMBLY COMPRISING LOCKABLE SYSTEMS," currently U.S. Patent Application Publication No. 2016/0174969;
-U.S. Patent Application No. 14 / 575,139, entitled "DRIVE ARRANGEMENTS FOR ARTICULATABLE SURGICAL INSTRUMENTS", currently U.S. Patent Application Publication No. 2016/0174978;
-U.S. Patent Application No. 14 / 575,148, entitled "LOCKING ARRANGEMENTS FOR DETACHABLE SHAFT ASSEMBLYES WITH ARTICULATABLE SURGICAL END EFFECTORS", now U.S. Patent Application Publication No. 2016/0149.
-U.S. patent application Ser. No. 14 / 575,130, entitled "SURGICAL INSTRUMENT WITH WITH AN ANVIL THAT IS SELECTIVELY MOVABLE ABOUT A DISCRETE NON-MOVABLE AXIS RELATIVE TOA TRAVEL PORTER TRACE AUTHOR TRAVEL TOP LAST ATOP REGARD TO A LAST GALLERY TO GIRL ,
-U.S. Patent Application No. 14 / 575,143, entitled "SURGICAL INSTRUMENTS WITH IMPROVED CLOSURE ARRANGEMENTS", currently U.S. Patent Application Publication No. 2016/0174983;
-U.S. patent application Ser. No. 14 / 575,117, entitled "SURGICAL INSTRUMENTS WITH ARTICULATABLE END EFFECTORS AND MOVABLE FIRING BEAM SUPPORT ARRANGEMENTS", now US Pat.
-U.S. patent application Ser. No. 14 / 575,154, entitled "SURGICAL INSTRUMENTS WITH ARTICULATABLE END EFFECTORS AND IMPROVED FIRING BEAM SUPPORT ARRANGEMENTS", now US Pat.
-U.S. Patent Application No. 14 / 574,493, entitled "SURGICAL INSTRUMENT ASSEMBLY COMPRISING A FLEXIBLE ARTICULATION SYSTEM", currently U.S. Patent Application Publication No. 2016/0174970, and-U.S. Patent Application No. 14 / 574,500. The title of the invention is "SURGICAL INSTRUMENT ASSEMBLY COMPRISING A LOCKABLE ARTICULATION SYSTEM", currently U.S. Patent Application Publication No. 2016/0174971.

The applicant of the present application owns the following patent applications filed on March 1, 2013, each of which is hereby incorporated by reference in its entirety:
-U.S. Patent Application No. 13 / 782,295, titled "ARTICULABLE SURGICAL INSTRUMENTS WITH CONDUCTIVE PATHWAYS FOR SIGNAL COMMUNICATION", now U.S. Patent Application Publication No. 2014/0246461,
-U.S. patent application Ser. No. 13 / 782,323, entitled "ROTARY POWERED ARTICULATION JOINTS FOR SURGICAL INSTRUMENTS", currently U.S. Patent Application Publication No. 2014/0246472,
-U.S. patent application Ser. No. 13 / 782,338, entitled "THUMMBHEEL SWITCH ARRANGEMENTS FOR SURGICAL INSTRUMENTS", currently U.S. Pat. Application Publication No. 2014/02494957;
-U.S. Patent Application No. 13 / 782,499, entitled "ELECTROMECHANICAL SURGICAL DEVICE WITH SIGNAL RELAY ARRANGEMENT," currently U.S. Patent No. 9,358,003,
U.S. Patent Application No. 13 / 782,460, entitled "MULTIPLE PROCESSOR MOTOR CONTROL FOR MODULAR SURGICAL INSTRUMENTS", currently U.S. Patent Application Publication No. 2014/0246478,
-U.S. Patent Application No. 13 / 782,358, entitled "JOYSTICK SWITCH ASSEMBLYES FOR SURGICAL INSTRUMENTS", currently U.S. Patent No. 9,326,767;
-U.S. patent application Ser. No. 13 / 782,481, entitled "SENSOR STRAIGHTENED END EFFECTOR DURING REMOVAL THROUGH TROCAR", now U.S. Pat. No. 9,468,438;
-U.S. Patent Application No. 13 / 782,518, entitled "CONTROL METALDS FOR SURGICAL INSTRUMENTS WITH REMOVABLE IMPLEMENT PORTIONS", currently U.S. Patent Application Publication No. 2014/0246475;
-U.S. patent application Ser. No. 13 / 782,375, entitled "ROTARY POWERED SURGICAL INSTRUMENTS WITH MULTIPLE DEGREES OF FREEDOM", currently U.S. Pat. No. 9,398,911, and-U.S. Pat. Application No. 13 / 782,536 No., title of invention "SURGICAL INSTRUMENT SOFT STOP", currently U.S. Pat. No. 9,307,986.

The applicant of the present application also owns the following patent applications filed on March 14, 2013, the entire contents of which are each incorporated herein by reference:
-U.S. Patent Application No. 13 / 803,097, entitled "ARTICULABLE SURGICAL INSTRUMENT COMPRISING A FIRING DRIVE", currently U.S. Patent Application Publication No. 2014/0263542,
-U.S. patent application Ser. No. 13 / 803,193, entitled "CONTROL ARRANGEMENTS FOR A DRIVE MEMBER OF A SURGICAL INSTRUMENT," currently U.S. Pat. No. 9,332,987;
U.S. patent application Ser. No. 13 / 803,053, title of invention "INTERCHANGEABLE SHAFT ASSEMBLYES FOR US WITH A SURGICAL INSTRUMENT", currently U.S. Patent Application Publication No. 2014/0263564;
U.S. Patent Application No. 13 / 803,086, entitled "ARTICULABLE SURGICAL INSTRUMENT COMPRISING AN ARTICULATION LOCK", currently U.S. Patent Application Publication No. 2014/0263541,
-U.S. Patent Application No. 13 / 803,210, entitled "SENSOR ARRANGEMENTS FOR ABSOLUTE POSITIONING SYSTEM FOR SURGICAL INSTRUMENTS", currently U.S. Patent Application Publication No. 2014/0263538,
-U.S. Patent Application No. 13 / 803,148, entitled "MULTI-FUNCTION MOTOR FOR A SURGICAL INSTRUMENT", currently U.S. Patent Application Publication No. 2014/0263554;
U.S. Patent Application No. 13 / 803,066, entitled "DRIVE SYSTEM LOCKOUT ARRANGEMENTS FOR MODULAR SURGICAL INSTRUMENTS", currently U.S. Patent Application Publication No. 2014/0263565;
-U.S. Patent Application No. 13 / 803,117, entitled "ARTICULATION CONTROL SYSTEM FOR ARTICULATABLE SURGICAL INSTRUMENTS", currently U.S. Patent No. 9,351,726;
-U.S. Patent Application No. 13 / 803,130, entitled "DRIVE TRAIN CONTROL ARRANGEMENTS FOR MODULAR SURGICAL INSTRUMENTS", currently U.S. Patent No. 9,351,727, and-U.S. Patent Application No. 13 / 803,159. The title of the invention is "METHOD AND SYSTEM FOR OPERATING A SURGICAL INSTRUMENT", currently U.S. Patent Application Publication No. 2014/0277017.

The applicant of the present application also owns the following patent application, filed March 7, 2014, the entire contents of which are incorporated herein by reference:
-U.S. Patent Application No. 14 / 200,111, entitled "CONTROL SYSTEMS FOR SURGICAL INSTRUMENTS", now U.S. Patent Application Publication No. 2014/0263539.

The applicant of the present application also owns the following patent applications filed on March 26, 2014, the entire contents of which are each incorporated herein by reference:
-U.S. Patent Application No. 14 / 226,106, entitled "POWER MANAGEMENT CONTROL SYSTEMS FOR SURGICAL INSTRUMENTS", currently U.S. Patent Application Publication No. 2015/0275258,
-U.S. Patent Application No. 14 / 226,099, entitled "STERILIZATION VERIFICATION CIRCUIT", currently U.S. Patent Application Publication No. 2015/0272581,
-U.S. Patent Application No. 14 / 226,094, entitled "VERIFICATION OF NUMBER OF BATTERY EXCHANGES / PROCEDURE COUNT", currently U.S. Patent Application Publication No. 2015/0272580,
-U.S. Patent Application No. 14 / 226,117, entitled "POWER MANAGEMENT THROUGH SLEEP OPTIONS OF SEGMENTED CIRCUIT AND WAKE UP CONTROL", currently U.S. Patent Application Publication No. 2015/0272574,
U.S. Patent Application No. 14 / 226,075, entitled "MODULAR POWERED SURGICAL INSTRUMENT WITH DETACHABLE SHAFT ASSEMBLIES", currently U.S. Patent Application Publication No. 2015/0272579,
-U.S. Patent Application No. 14 / 226,093, entitled "FEEDBACK ALGORITHMS FOR MANUAL BAILOUT SYSTEMS FOR SURGICAL INSTRUMENTS", currently U.S. Patent Application Publication No. 2015/0272569,
-U.S. Patent Application No. 14 / 226,116, entitled "SURGICAL INSTRUMENT UTILIZING SENSOR ADAPTATION", currently U.S. Patent Application Publication No. 2015/0272571,
-U.S. Patent Application No. 14 / 226,071, entitled "SURGICAL INSTRUMENT CONTROL CIRCUIT HAVING A SAFETY PROCESSOR", currently U.S. Patent Application Publication No. 2015/0272578;
-U.S. Patent Application No. 14 / 226,097, entitled "SURGICAL INSTRUMENT COMPRISING INTERACTIVE SYSTEMS," currently U.S. Patent Application Publication No. 2015/0272570,
-U.S. Patent Application No. 14 / 226,126, entitled "INTERFACE SYSTEMS FOR USE WITH SURGICAL INSTRUMENTS", currently U.S. Patent Application Publication No. 2015/0272572,
-U.S. Patent Application No. 14 / 226,133, titled "MODULAR SURGICAL INSTRUMENT SYSTEM", currently U.S. Patent Application Publication No. 2015/0272557;
-U.S. patent application Ser. No. 14 / 226,081, entitled "SYSTEMS AND METHODS FOR CONTROL A SEGMENTED CIRCUIT", currently U.S. Patent Application Publication No. 2015/0277471;
-U.S. Patent Application No. 14 / 226,076, entitled "POWER MANAGEMENT THROUGH SEGMENTED CIRCUIT AND VARIABLE VOLTAGE PROTECTION", currently U.S. Patent Application Publication No. 2015/0280424;
-U.S. Patent Application No. 14 / 226,111, title of the invention "SURGICAL STAPLING INSTRUMENT SYSTEM", currently U.S. Patent Application Publication No. 2015/0272583, and-U.S. Patent Application No. 14 / 226,125, "SURGICAL INSTRUMENT COMPRISING A ROTATABLE SHAFT", currently U.S. Patent Application Publication No. 2015/0280384.

The applicant of the present application also owns the following patent applications filed on September 5, 2014, each of which is hereby incorporated by reference in its entirety:
-U.S. patent application Ser. No. 14 / 479,103, entitled "CIRCUITRY AND SENSORS FOR POWERED MEDICAL DEVICE", currently U.S. Patent Application Publication No. 2016/0066912,
-U.S. Patent Application No. 14 / 479,119, entitled "ADJUNCT WITH INTEGRATED SENSORS TO QUANTIFY TISSUE COMPRESSION", currently U.S. Patent Application Publication No. 2016/0066914;
-U.S. Patent Application No. 14 / 478,908, entitled "MONITORING DEVICE DEGRADATION BASED ON COMPONENT EVALUATION," currently U.S. Patent Application Publication No. 2016/0066910,
-U.S. Patent Application No. 14 / 478,895, entitled "MULTIPLE SENSORS WITH ONE SENSOR AFFECTING A SECOND SENSOR'S OUTPUT OR INTERPRETATION", now U.S. Patent Application Publication No. 2016/0066909;
-U.S. Patent Application No. 14 / 479,110, entitled "POLARITY OF HALL MAGNET TO DETECT MISLOADED CARTRIDGE", currently U.S. Patent Application Publication No. 2016/0066915,
-U.S. Patent Application No. 14 / 479,098, entitled "SMART CARTRIDGE WAKE UP OPERATION AND DATA RETENTION," currently U.S. Patent Application Publication No. 2016/0066911,
-U.S. Patent Application No. 14 / 479,115, titled "MULTIPLE MOTOR CONTROL FOR POWERED MEDICAL DEVICE", currently U.S. Patent Application Publication No. 2016/0066916, and-U.S. Patent Application No. 14 / 479,108, The name of the invention, "LOCAL DISPLAY OF TISSUE PARAMETER STABILIZATION", currently US Patent Application Publication No. 2016/0066913.

The applicant of the present application also owns the following patent applications filed on April 9, 2014, the entire contents of which are each incorporated herein by reference:
U.S. Patent Application No. 14 / 248,590, entitled "MOTOR DRIVEN SURGICAL INSTRUMENTS WITH LOCKABLE DUAL DRIVE SHAFTS", currently U.S. Patent Application Publication No. 2014/0305987;
-U.S. Patent Application No. 14 / 248,581, entitled "SURGICAL INSTRUMENT COMPRISING A CLOSING DRIVE AND A FIRING DRIVE OPERATED FROM THE SAME ROTATABLE OUTPUT," currently US Patent Application No. 305, U.S. Pat.
-U.S. Patent Application No. 14 / 248,595, entitled "SURGICAL INSTRUMENT SHAFT INCLUDING SWITCHES FOR CONTROL LING THE OPERATION OF THE THE SURGITAL INSTRUMENT", now U.S. Pat.
-U.S. Patent Application No. 14 / 248,588, entitled "POWERED LINEAR SURGICAL STAPLER", currently U.S. Patent Application Publication No. 2014/0309666,
-U.S. Patent Application No. 14 / 248,591, entitled "TRANSMISSION ARRANGEMENT FOR A SURGICAL INSTRUMENT", currently U.S. Patent Application Publication No. 2014/0305991,
-U.S. patent application Ser. No. 14 / 248,584, entitled "MODULAR MOTOR DRIVEN SURGICAL INSTRUMENTS WITH ALIGNMENT FEATURES FOR ALIGNING ROTARY ROTARY DRIVE SHAFTS WITH SERVICES RIGHT SERVICES RIGHT SERVICES RIGHT SERVICES RIGHT RIGHT SERVICES RIGHT SERVICES RIGHT SERVICES RIGHT SERVICES RIGHT SERVICES CURRENT SERVICES CURRENT SERVICES CURRENT SERVICES CURRENT SERVICES CURRENT SERVICES CURRENT SERVICES CURRENT SERVICES CURRENT SERVICES CURRENT SERVICES CURRENT SERVICES CURRENT SERVICES U.S. Pat.
-U.S. Patent Application No. 14 / 248,587, entitled "POWERED SURGICAL STAPLLER", currently U.S. Patent Application Publication No. 2014/0309665,
-U.S. Patent Application No. 14 / 248,586, title of invention "DRIVE SYSTEM DECOUPLING ARRANGEMENT FOR A SURGICAL INSTRUMENT", currently U.S. Patent Application Publication No. 2014/0305990, and-U.S. Patent Application No. 14 / 248,607. The title of the invention is "MODULAR MOTOR DRIVEN SURGICAL INSTRUMENTS WITH STATUS INDICATION ARRANGEMENTS", currently US Patent Application Publication No. 2014/0305992.

The applicant of the present application also owns the following patent applications filed on April 16, 2013, each of which is hereby incorporated by reference in its entirety:
-US Provisional Patent Application No. 61 / 812,365, entitled "SURGICAL INSTRUMENT WITH MULTIPLE FUNCTIONS PERFORMED BY A SINGLE MOTOR",
-U.S. Provisional Patent Application No. 61 / 812,376, entitled "LINEAR CUTTER WITH POWER",
-U.S. Provisional Patent Application No. 61 / 812,382, entitled "LINEAR CUTTER WITH MOTOR AND PISTOL GRIP",
-U.S. Provisional Patent Application No. 61 / 812,385, title of the invention "SURGICAL INSTRUMENT HANDLE WITH WULT MULTIPLE ACTUATION MOTORS AND MOTOR CONTROL," and-U.S. Provisional Patent Application No. 61 / 812,372, title of invention "SUNRTIG MULTIPLE FUNCTIONS PERFORMED BY A SINGLE MOTOR ".

  As set forth in the specification and illustrated in the accompanying drawings, numerous specific details are set forth in order to provide a thorough understanding of the overall structure, function, manufacture, and use of the embodiments. Well-known operations, components and elements have not been described in detail so as not to obscure the embodiments described herein. The reader is advised that the embodiments described and illustrated herein are non-limiting examples, and thus certain structural and functional details disclosed herein may be representative and illustrative. You will understand. Modifications and changes may be made thereto without departing from the scope of the claims.

  The terms "comprise" (any form of comprises, such as "comprises" and "comprising"), "have" (any form of have, such as "has" and "having"), "include ( include) "(any word form of include, such as" includes "and" including "), and" contain "(any word form of container, such as" contains "and" containing ") are open-ended concatenations. Verb. As a result, a surgical system, device, or apparatus that “comprises,” “has,” “includes,” or “contains” one or more elements has one or more of those elements. But not limited to having only one or more of them. Similarly, an element of a system, device, or apparatus that “comprises,” “has,” “includes,” or “contains” one or more features has one or more of those features. But not limited to having only one or more of these features.

  The terms "proximal" and "distal" are used herein with reference to a clinician operating the handle portion of a surgical instrument. The term "proximal" refers to the portion closest to the clinician, and the term "distal" refers to the portion remote from the clinician. It will be further understood that for convenience and clarity, spatial terms such as "vertical", "horizontal", "top", and "bottom" may be used herein with respect to the drawings. However, surgical instruments are used in many orientations and positions, and these terms are not intended to be limiting and / or absolute.

  Various exemplary devices and methods are provided for performing laparoscopic and minimally invasive surgery. However, the reader will readily appreciate that the various methods and devices disclosed herein may be used in many surgical procedures and applications, including those associated with open surgery. By reading through the Detailed Description of the Invention herein, the reader will appreciate that various instruments disclosed herein can be used, for example, through incisions or punctures made in tissue through natural orifices. It will be further appreciated that it can be inserted into the body in any manner, such as through a hole. The working or end effector portion of these instruments can be inserted directly into the patient's body, or inserted through an access device that has a working channel through which the end effector and elongate shaft of the surgical instrument can be advanced. You can also.

  A surgical stapling system can include a shaft and an end effector extending from the shaft. The end effector includes a first jaw and a second jaw. The first jaw includes a staple cartridge. Other implementations in which the staple cartridge is insertable into and removable from the first jaw, but the staple cartridge is not removable from the first jaw or at least not easily replaceable Forms are also envisioned. The second jaw includes an anvil configured to deform staples ejected from the staple cartridge. The second jaw is pivotable about the closing axis with respect to the first jaw, although other embodiments are contemplated where the first jaw is pivotable with respect to the second jaw. Is done. The surgical stapling system further comprises an articulation configured to allow the end effector to rotate, ie, articulate, relative to the shaft. The end effector is rotatable about an articulation axis extending through the articulation. Other embodiments that do not include an articulation are also contemplated.

  The staple cartridge includes a cartridge body. The cartridge body includes a proximal end, a distal end, and a deck extending between the proximal and distal ends. In use, the staple cartridge is positioned on a first side of the tissue to be stapled and the anvil is positioned on a second side of the tissue. The anvil is moved toward the staple cartridge to compress and clamp tissue against the deck. Subsequently, the staple removably stored in the cartridge body can be deployed in the tissue. The cartridge body includes a staple cavity defined therein, and the staple is removably stored within the staple cavity. The staple cavities are arranged in six longitudinal rows. Three rows of staple cavities are located on a first side of the longitudinal slot, and three rows of staple cavities are located on a second side of the longitudinal slot. Other arrangements of staple cavities and staples may also be possible.

  The staples are supported by a staple driver in the cartridge body. The driver is movable between a first, or unfired position, and a second, or fired, position that ejects staples from the staple cavity. The driver includes an elastic member retained within the cartridge body by a retainer extending around a bottom of the cartridge body and configured to grip the cartridge body and retain the retainer relative to the cartridge body. . Drivers are movable by a sled between their unfired position and their fired position. The sled is movable between a proximal position adjacent the proximal end and a distal position adjacent the distal end. The sled includes a plurality of ramps configured to slide beneath the driver and lift the driver, with staples supported thereon and toward the anvil.

  In addition to the above, the sled is moved distally by the firing member. The firing member is configured to contact the sled and push the sled toward the distal end. A longitudinal slot defined in the cartridge body is configured to receive a firing member. The anvil also includes a slot configured to receive the firing member. The firing member further includes a first cam that engages the first jaw, and a second cam that engages the second jaw. As the firing member is advanced in the distal direction, the first and second cams can control the distance between the staple cartridge deck and the anvil, ie, the tissue gap. The firing member also includes a knife configured to cut tissue captured between the staple cartridge and the anvil. It is desirable that the knife be positioned at least partially proximal to the ramp so that the staples are ejected forward of the knife.

  FIG. 1 illustrates one form of a replaceable surgical tool assembly 1000 operably coupled to a motorized handle assembly 500. The replaceable surgical tool assembly 1000 can also be effectively used with a tool drive assembly of a robotic or automated surgical system. For example, the surgical tool assembly disclosed herein is disclosed in U.S. Patent No. 9,072,535, entitled "SURGICAL STAPLING INSTRUMENTS WITH ROTATABLE STAPLE DEPLOYMENT ARRANGEMENTS," which is incorporated herein by reference in its entirety. It can be used with various robotic systems, instruments, components, and methods, such as, but not limited to, those disclosed. The handle assembly 500, as well as the tool drive assembly of the robot system, may also be referred to herein as a "control system" or "control unit."

  FIG. 2 illustrates the attachment of the replaceable surgical tool assembly 1000 to the handle assembly 500. The handle assembly 500 may include a handle housing 502 that includes a pistol grip portion 504 that can be grasped and manipulated by a clinician. Handle assembly 500 may further include a frame 506 operably supporting a plurality of drive systems. For example, the frame 506 can operably support a “first” or closed drive system, generally indicated as 510, which is operably attached to or coupled to the handle assembly 500. The interchangeable surgical tool assembly 1000 can be used to apply an opening and closing motion. In at least one form, the closure drive system 510 may include an actuator in the form of a closure trigger 512 pivotally supported by the frame 506. Such a mechanism allows the clinician to operate the closure trigger 512 so that, when the clinician grips the pistol grip portion 504 of the handle assembly 500, the closure trigger 512 is moved to a start position or an "inactive" position. From the "actuated" position, more specifically the fully compressed or fully activated position. In various forms, the closure drive system 510 further includes a closure linkage 514 pivotally coupled to, or otherwise operably interfaced with, the closure trigger 512. As will be described in further detail below, in the illustrated example, the closure link mechanism 514 includes a lateral mounting pin 516 that facilitates mounting to a corresponding drive system on the surgical tool assembly. In use, to activate the closure drive system 510, the clinician presses the closure trigger 512 toward the pistol grip portion 504. Further details are found in U.S. Patent Application No. 14 / 226,142, entitled "SURGICAL INSTRUMENT COMPRISING A SENSOR SYSTEM", now U.S. Patent Application Publication No. 2015/0272575, which is incorporated herein by reference in its entirety. As described, the closure drive system 510 is configured to lock the closure trigger 512 in the fully-pressed or fully-actuated position when the clinician fully presses the closure trigger 512 to achieve a “full” closure stroke. You. If the clinician desires to unlock and bias the closure trigger 512 to the inactive position, the clinician simply activates the closure release button assembly 518, thereby returning the closure trigger 512 to the inactive position. It becomes possible. The closure release button assembly 518 may also be configured to interact with various sensors in communication with the microcontroller 520 in the handle assembly 500 to track the position of the closure trigger 512. Further details regarding the construction and operation of the closure release button assembly 518 can be found in US Patent Application Publication No. 2015/0272575.

  In at least one form, the handle assembly 500 and the frame 506 are configured to apply an axial or firing motion to a corresponding portion of the replaceable surgical tool assembly attached thereto, the firing herein. Another drive system, referred to as drive system 530, may be operably supported. The firing drive system 530 may employ an electric motor 505 located within the pistol grip portion 504 of the handle assembly 500, as described in more detail in US Patent Application Publication No. 2015/0272575. In various embodiments, the motor 505 may be, for example, a brushed DC drive motor having a maximum speed of about 25,000 RPM. In another arrangement, motor 505 may include a brushless motor, a cordless motor, a synchronous motor, a stepper motor, or any other suitable electric motor. The motor 505 may be powered by a power source 522, which in one form may include a removable power pack. The power pack can support a plurality of lithium ion ("LI") or other suitable batteries therein. Many batteries that can be connected in series can be used as power source 522 for handle assembly 500. In addition, power supply 522 may be replaceable and / or rechargeable.

  The electric motor 505 is configured to axially drive a longitudinally movable drive member 540 in a distal direction and a proximal direction depending on the polarity of the motor. For example, when the motor 505 is driven in a rotational direction, the longitudinally movable drive member 540 will be driven axially in the distal direction "DD". When the motor 505 is driven in the opposite rotational direction, the longitudinally movable drive member 540 will be driven axially in the proximal direction "PD". Handle assembly 500 can include a switch 513 that can be configured to reverse the polarity applied to electric motor 505 by power supply 522 or otherwise control motor 505. Handle assembly 500 may also include a sensor or sensors (not shown) configured to detect the position of drive member 540 and / or the direction in which drive member 540 is being moved. Operation of the motor 505 may be controlled by a firing trigger 532 pivotally supported on the handle assembly 500. The firing trigger 532 may be pivoted between an inactive position and an active position. The firing trigger 532 can be biased to a non-activated position by a spring (not shown) or other biasing mechanism so that when the clinician releases the firing trigger 532, the firing trigger 532 is It can be pivoted to the inoperative position by the biasing arrangement or returned in another way. In at least one form, firing trigger 532 may be positioned “outside” closing trigger 512, as described above. As discussed in U.S. Patent Application Publication No. 2015/0272575, handle assembly 500 may include a firing trigger safety button (not shown) to prevent accidental activation of firing trigger 532. . When the closure trigger 512 is in the inactive position, the safety button is housed within the handle assembly 500, the clinician cannot easily touch the safety button, and has a safety position that prevents actuation of the firing trigger 532. The safety button cannot be moved between the firing position where the firing trigger 532 can be fired. When the clinician depresses the closure trigger 512, the safety button and the firing trigger 532 may pivot downward, allowing them to be subsequently operated by the clinician.

  In at least one form, the longitudinally movable drive member 540 includes a toothed rack formed thereon for mating engagement with a corresponding drive gear mechanism (not shown) that interfaces with the motor 505. (Not shown). Further details regarding these features can be found in US Patent Application Publication No. 2015/0272575. At least one configuration includes a manually actuated “emergency disengagement” configured to allow the clinician to manually retract the longitudinally movable drive member 540 if the motor 505 becomes unavailable. An assembly. The emergency release assembly may include a lever or emergency release handle assembly stored within handle assembly 500 under releasable door 550. The lever is configured to be manually pivoted into ratchet engagement with the teeth of the drive member 540. Accordingly, the clinician can manually retract the drive member 540 by ratcheting the drive member 540 in the proximal direction "PD" using the emergency release handle assembly. U.S. Patent Application Publication No. 12 / 249,117, entitled "POWERED SURGICAL CUTTING AND STAPLING APPARATUS WITH MANUALLY RETRACTABLE FIRING SYSTEM", now incorporated by reference in U.S. Pat. 008970) discloses an emergency release mechanism and other components, mechanisms, and systems that can also be used with the tool assembly 1000.

  Referring now to FIGS. 5 and 6, the replaceable surgical tool assembly 1000 includes a shaft mounting portion 1300 operably attached to an elongate shaft assembly 1400. A surgical end effector 1100 including an elongate channel 1102 configured to operably support a surgical staple cartridge 1150 therein is operably attached to an elongate shaft assembly 1400. See FIGS. 3 and 6. Surgical end effector 1100 may further include an anvil 1130 pivotally supported with respect to elongate channel 1102. The elongated channel 1102 with the staple cartridge 1150 installed therein, and the anvil 1130 may also be referred to as the "jaw" of the end effector. The replaceable surgical tool assembly 1000 can be configured to releasably hold the surgical end effector 1100 at a desired articulated position about an articulation axis BB transverse to the shaft axis SA. It may further include an articulation 1200 and an articulation lock 1210 (FIGS. 3 and 6). For more details regarding the structure and operation of the articulation lock 1210, see U.S. Patent Application Publication No. 13 / 803,086, entitled "ARTICULATEABLE SURGICAL INSTRUMENT COMPRISING AN ARTICULATION LOCK", the disclosure of which is incorporated herein by reference in its entirety. , Can be found in the current US Patent Application Publication No. 2014/0263541. For further details regarding the articulation lock 1210, see U.S. Patent Application Serial No. 15 / 019,196, filed February 9, 2016, entitled "SURGICAL INSTRUMENT ARTICULATION MECHANISM WITH SLOTTED," filed February 9, 2016, the entire disclosure of which is incorporated herein by reference. SECONDARY CONSTRAINT ".

  As can be seen in FIGS. 5 and 6, the shaft mounting portion 1300 includes a proximal housing or nozzle 1301 composed of nozzle portions 1302, 1304 and a clasp, lug, screw, etc., on the assembled nozzle portions 1302, 1304. An actuator wheel portion 1306 configured to be coupled. In the illustrated embodiment, the replaceable surgical tool assembly 1000 may be utilized to close and / or open the anvil 1130 relative to the elongate channel 1102 of the surgical end effector 1100, as discussed in further detail below. Further includes a closure assembly 1406. In addition, the illustrated replaceable surgical tool assembly 1000 includes a spine assembly 1500 that operatively supports the articulation lock 1210. The spine 1500 may first slidably support the firing member assembly 1600 therein, and secondly extend around the spine assembly 1500 or otherwise movably supported by the spine assembly 1500. Configured to slidably support the configured closure assembly 1406.

  In the mechanism shown, the surgical end effector 1100 is operatively connected to the elongate shaft assembly 1400 by an articulation joint 1200, which is centered about an articulation axis BB transverse to the shaft axis SA. Facilitates selective articulation of the configured surgical end effector 1100. Please refer to FIG. As seen in FIGS. 5 and 6, spine assembly 1500 slidably supports proximal articulation driver 1700 operatively interface with articulation lock 1210. The articulation lock 1210 is supported on a distal frame segment 1560 that further includes a portion of the spine assembly 1500. As seen in FIG. 6, the distal frame segment 1560 includes a distal spine extension 1562 pivotally connected to the elongate channel 1102 by an end effector mounting assembly 1230. In one arrangement, for example, the distal end 1563 of the distal frame segment 1560 has a spine mounting pin 1564 formed thereon. Spine mounting pins 1564 are adapted to be pivotally received in spine mounting holes 1234 formed in end effector mounting assembly 1230. Please refer to FIG.

  Referring again to FIG. 6, in the illustrated embodiment, the proximal articulation driver 1700 has a distal end 1702 configured to operably engage the articulation lock 1210. The articulation lock 1210 includes an articulation frame 1212 that is pivotally coupled or pinned to a distal articulation link 1710 that is also configured to be pivotally attached to the end effector mounting assembly 1230. Specifically, as seen in FIG. 6, the distal end 1712 of the distal articulation link 1710 is adapted to be pivotally received in a corresponding articulation hole 1236 in the end effector mounting assembly 1230. Includes a configured articulation pin 1714. Distal articulation link 1710 is slidably supported by distal spine extension 1562. End effector mounting assembly 1230 extends through a lateral mounting hole 1231 in end effector mounting assembly 1230 and is received in a channel or jaw mounting hole 1106 provided at proximal end 1103 of elongate channel 1102. Attached to the proximal end 1103 of the elongate channel 1102 by a spring pin connector 1235. Spine mounting pin 1564 defines an articulation axis BB transverse to shaft axis SA. Such a mechanism facilitates pivotal movement (i.e., articulation) of the surgical end effector 1100 about the articulation axis BB relative to the spine assembly 1500. As discussed above, further details regarding the operation of the articulation lock 1210 and articulation frame 1212 can be found in U.S. Patent Application No. 13 / 803,086, and current U.S. Patent Application Publication No. 2014/0263541.

  In various situations, spine assembly 1500 further includes an intermediate spine segment 1510 attached to distal frame segment 1560 of joint lock 1210. The spine assembly 1500 has opposing notches 1535 (only one is visible in FIG. 5) for receiving a corresponding mounting lug 1308 (shown in FIG. 4) projecting inward from each of the nozzle portions 1302, 1304. ) Further includes a proximal spine mounting segment 1530 that includes a proximal end portion 1532 having a Such a mechanism facilitates rotation of the proximal spine assembly 1500 about the shaft axis SA by rotating the nozzle 1301 about the shaft axis SA. Replaceable surgical tool assembly 1000 includes a chassis 1800 that rotatably supports shaft assembly 1400. The proximal end portion 1532 of the proximal spine mounting segment is rotatably supported in a central shaft hole 1801 formed in the chassis 1800. Please refer to FIG. In one arrangement, for example, the proximal end portion 1532 may be mounted thereon for spine bearings (not shown) or otherwise supported within spine bearings mounted within the chassis 1800. Have a thread 1533. Such a mechanism facilitates rotatable attachment of spine assembly 1500 to chassis 1800, thereby allowing spine assembly 1500 to be selectively rotated relative to chassis 1800 about shaft axis SA.

  The closure assembly 1406 includes an elongated proximal closure member 1410 and a distal closure member 1430. In the mechanism shown, proximal closure member 1410 includes a hollow tubular member slidably supported on spine assembly 1500. Accordingly, proximal closure member 1410 may also be referred to herein as a "proximal closure tube." Similarly, distal closure member 1430 may also be referred to as a “distal closure tube”. Referring primarily to FIG. 5, the replaceable surgical tool assembly 1000 includes a closed shuttle 1420 slidably supported within the chassis 1800 so that it can be moved axially relative to the chassis 1800. In one form, closure shuttle 1420 includes a pair of proximally protruding hooks 1421 configured to attach to a lateral attachment pin 516 (FIG. 2) that attaches to closure link tackle assembly 514 of handle assembly 500. Thus, when hook 1421 is hooked on lateral mounting pin 516, actuation of closure trigger 512 causes axial movement of closure shuttle 1420, and ultimately closure assembly 1406, on spine assembly 1500. A closure spring (not shown) may also be journaled on closure sleeve 1406 and serves to bias closure assembly 1406 in a proximal direction “PD”, such that surgical tool assembly 1000 may handle handle assembly 500. When operably coupled to the lock, it may serve to pivot the closure trigger 512 to a non-actuated position. In use, closure assembly 1406 is translated distally (direction DD) to close jaws 1130, 1102, for example, in response to actuation of closure trigger 512.

  The closing link mechanism 514 may also be referred to herein as a "closing actuator", and the closing link mechanism 514 and the closing shuttle 1420 may be collectively referred to herein as a "closing actuator assembly". Proximal end 1412 of proximal closure member 1410 is coupled to closure shuttle 1420 for relative rotation therewith. For example, a U-shaped connector 1424 is inserted into an annular slot 1414 at the proximal end 1412 of the proximal closure member 1410 and is retained within a vertical slot 1422 of the closure shuttle 1420. Please refer to FIG. Such a mechanism serves to attach the proximal closure member 1410 to the closure shuttle 1420 for axial movement with the closure shuttle 1420, while the closure assembly 1406 rotates relative to the closure shuttle 1420 about the shaft axis SA. Enable.

  As described above, the illustrated interchangeable surgical tool assembly 1000 includes the articulation 1200. As seen in FIG. 6, the upper and lower tangs 1415, 1416 project distally from the distal end of the proximal closure member 1410 and are movably connected to the distal closure member 1430. As further seen in FIG. 6, distal closure member 1430 includes upper and lower protrusions 1434, 1436 projecting proximally from its proximal end. Proximal closure member 1410 and distal closure member 1430 are connected together by an upper double pivot link 1220. Upper double pivot link 1220 includes proximal and distal pins that engage corresponding holes in upper protrusions 1415, 1434 of proximal closure member 1410 and distal closure member 1430, respectively. The proximal closure member 1410 and the distal closure member 1430 are also connected together by a lower double pivot link 1222. The lower dual pivot link 1222 includes proximal and distal pins that engage corresponding holes in the lower protrusions 1416 and 1436 of the proximal and distal closure members 1410 and 1430, respectively. As discussed in further detail below, distal and proximal axial translation of closure assembly 1406 causes opening and closing of anvil 1130.

  The replaceable surgical tool assembly 1000 shown in FIGS. 1-6 includes a surgical end effector 1100 capable of articulating in one direction about an articulation axis BB. As described above, the articulation axis BB is defined by spine mounting pins 1564 rotatably received in spine mounting holes 1234 formed in end effector mounting assembly 1230. In the illustrated mechanism, the spine mounting holes 1234 may be transversely axially aligned with the shaft axis SA. In other arrangements, the spine mounting holes 1234 may be slightly laterally offset from the shaft axis. In the example shown, the articulation axis BB crosses and intersects the shaft axis SA. The depicted example is a proximal articulation drive that interfaces (via articulation lock 1210) with a single distal articulation link 1710 that operatively interfaces with and applies articulation to the end effector mounting assembly 1230. Only the vessel 1700 is used. For example, advancing distal articulation link 1710 distally causes surgical end effector 1100 to articulate in a single “first” articulation direction. In one mechanism, for example, the surgical end effector 1100 may be selectively articulatable from a first non-articulated position, and the surgical end effector 1100 may have an articulation angle of about 110 degrees ( The surgical end effector 1100 is axially aligned with the shaft assembly 1400 (after the trocar exits the patient and into the patient) (for insertion through the trocar or other access opening). Other joint angle configurations can also be achieved.

  As seen in FIG. 7, for example, the replaceable surgical tool assembly 1000 may be suitable for use in connection with a medical procedure known as a lower anterior resection “LAR”. Such procedures generally involve the removal of lesions of the colon. For example, the treatment may include removing blood vessels and lymph nodes associated with this portion of the intestine. The surgeon then rejoins the remaining colon with the rest of the rectum (this may be referred to as an anastomosis). One challenge commonly encountered by surgeons during this procedure is related to placing the end effector deep enough into the pelvic region to complete the procedure. FIG. 7 illustrates the desired position of the surgical end effector 1100 within the patient's pelvis 400 upon resection of the patient's colon 410. The line BTL in FIG. 7 may indicate the movement limits typically provided by the patient's pelvic bone structure and associated tissue. In the mechanism shown, the surgical tool assembly 1000 uses a “asymmetric” proximal closure member 1410 configured to provide additional clearance and maneuverability within the area for the surgical tool assembly 1000. .

  As seen in FIG. 7, in one example, the proximal closure member 1410 of the shaft assembly 1400 includes an elongated proximal end portion 1417 and an elongated distal end portion 1411 extending from the proximal end portion 1417. As seen in FIGS. 7-9, an asymmetric cutout or notch area 1418 may be provided at the distal end portion 1411 of the proximal closure member 1410, for example, to facilitate greater clearance between the shaft assembly 1400 and the pelvic structure. Is provided. In at least one example, notch region 1418 extends throughout distal end portion 1411. In such a mechanism, the axial length of the distal end portion is shorter than the axial length of the proximal end portion 1417.

  Referring now to FIG. 11, in the illustrated example, the proximal end portion 1417 has an uninterrupted or “continuous” “proximal” outer circumference or outer shape 1417P. At least a portion of the distal end portion 1411 has a discontinuous or interrupted "distal" outer or outer peripheral shape 1411P. As further seen in FIG. 9, for example, the distal spine extension 1562 has a similar notch area 1568 therein. Also, intermediate spine segment 1510 may also have an asymmetric notch 1516 therein that coincides with notch regions 1418 and 1568. Please refer to FIG. 10 and FIG. Such a mechanism may allow a clinician to position shaft assembly 1400 and surgical end effector 1100 in the pelvic region at the positions shown in FIG. In the illustrated mechanism, for example, the joint angle AA may be about 110 degrees. Accordingly, such a mechanism may provide a clinician with the ability to position the surgical end effector 1100 deeper within the pelvic region as compared to other tools and end effector mechanisms. In the mechanism shown, the notch regions 1418, 1516, 1568 are located on the opposite side (eg, in the direction of the articulation DA) of the shaft axis SA from which the end effector 1100 articulates. However, in other arrangements, the notch regions 1418, 1516, 1568 may be provided on the same side of the shaft axis SA from which the surgical end effector articulates.

  In one embodiment, the proximal closure member 1410 moves axially over the spine assembly 1500 to maintain the proximal closure member 1410 axially aligned on the spine assembly 1500 and to move the end effector jaw. Opposing closure alignment members 1413 are used to slow or prevent buckling of shaft components during articulation and closure of 1130, 1102. In one arrangement, for example, a pair of diametrically opposed alignment pins 1413 are attached to and extend inward from the proximal closure member 1410 to provide an intermediate spine segment 1510 and a distal Each is slidably received in a corresponding alignment slot 1514, 1566 in the spine extension 1562. Please refer to FIG. 10 and FIG. As further seen in FIG. 11, the distal spine extension 1562 may have a recessed area 1567 for receiving a downwardly projecting lug portion 1518 formed under the intermediate spine segment 1510. . Such a mechanism may serve to laterally interlock the intermediate spine segment 1510 and the distal spine extension 1562 together, thereby creating any lateral deflection between these components. It can function to resist doing. FIG. 12 shows that the proximal closure member 1410 ′ can serve to limit any tendency of the upper and lower projections 1415, 1416 to spread apart during use. An alternative proximal closure member 1410 'is shown that is identical to the proximal closure member 1410 described above, except that it includes a connector bridge 1419 extending therebetween.

  FIG. 13 is configured to prevent or limit proximal closure member 1410 ″ from opening in direction OD when a lateral load LL is applied laterally to shaft assembly 1400 in the notch region. 3 shows another mechanism performed. Proximal closure member 1410 '' may be identical to proximal closure member 1410 except for the differences described herein. As seen in FIG. 13, the proximal closure member 1410 ″ further includes a pair of inwardly projecting, somewhat diametrically opposed bent tabs 1425. One flex tab 1425 is slidably received within a corresponding axially extending slot 1519 and the other flex tab 1425 is within a corresponding axial slot 1569 within the distal spine extension 1562. Slidably received. Such a mechanism slidably interlocks the proximal closure member 1410 ″ on the spine assembly 1500 ′ so that the proximal closure member 1410 ″ opens when a lateral load LL is applied. It plays the role of resisting (in the OD direction). FIG. 14 shows an alternative mechanism that is somewhat L-shaped and uses bent tabs 1425 'slidably received in corresponding L-shaped slots 1514' and 1569 '.

  As described above, the replaceable surgical tool assembly 1000 further includes a firing member assembly 1600 supported for axial movement within the spine assembly 1500. In the illustrated embodiment, firing member assembly 1600 includes a proximal firing shaft segment 1602 and a distal cutting portion or distal firing bar 1620. The firing member assembly 1600 may also be referred to herein as a “second shaft” and / or “second shaft assembly”. As seen in FIG. 5, proximal firing shaft segment 1602 projects proximally from its proximal end, and firing shaft mounting within a longitudinally movable drive member 540 supported within handle assembly 500. Includes a proximal mounting lug 1604 configured to be operably received within cradle 542. Please refer to FIG.

  Referring again to FIG. 5, the distal end 1606 of the proximal firing shaft segment 1602 includes a longitudinal slot 1608 configured to receive a tab (not shown) on the proximal end of the distal firing bar 1620. Including. The longitudinal slot 1608 and the proximal end of the distal firing bar 1620 may be sized and configured to allow relative movement therebetween, and may include a slip joint 1622. Sliding joint 1622 may move proximal firing shaft segment 1602 without moving, or at least substantially moving, distal firing bar 1620 during operation of the articulation. Once the end effector 1100 is properly oriented, the proximal firing shaft segment 1602 can be advanced distally until the proximal end wall of the slot 1608 contacts a tab on the distal firing bar 1620 to provide distal firing. Bar 1620 can be advanced to fire surgical staple cartridge 1150 positioned within elongate channel 1102. As further seen in FIG. 5, the intermediate spine segment 1510 includes a channel 1512 for slidably supporting the proximal firing shaft segment 1602 therein. The upper spine cover 1527 is engaged with the intermediate spine segment 1510 to facilitate assembly of the proximal firing shaft segment 1602 and the spine assembly 1500 to encapsulate these portions of the firing member assembly 1600. Good.

  FIG. 15 shows the surgical end effector 1100 in an articulated position. As seen in FIGS. 15 and 6, central support member 1614 provides lateral support to distal firing bar 1620 as it flexes to accommodate the articulation of surgical end effector 1100. Used to provide. In one embodiment, distal pivot pin 1615 projects from the distal end of central support member 1614 and is received within spine mounting hole 1234 of end effector mounting assembly 1230. Proximal pivot pin 1616 is received within elongated slot 1569 of distal spine extension 1562. Additionally, central support member 1614 includes a passageway 1618 therein that provides lateral support to distal firing bar 1620 when surgical end effector 1100 is articulating. Further details regarding the central support member and alternative knife bar support mechanisms are disclosed in U.S. Patent Application No. 15 / 019,245, which is incorporated herein by reference in its entirety.

  FIG. 15A illustrates an alternative articulation 1200 ′ that facilitates articulation of a surgical end effector 1100 about an articulation axis BB transverse to a shaft axis SA defined by an elongate shaft assembly 1400 ′. , An articulation 1200 ′ is operably attached to the elongated shaft assembly 1400 ′. In the illustrated example, the surgical end effector 1100 is selectively articulatable to one side of the shaft axis SA. Such joint movement directions are represented by arrows LD. As in the previous embodiment, the end effector mounting assembly 1230 is pivotally attached to the proximal end 1103 of the elongated channel 1102 of the surgical end effector 1100. End effector mounting assembly 1230 is pivotally mounted to distal spine extension 1562 of distal frame segment 1560 of elongate shaft assembly 1400 '. As in the previous embodiment, the distal frame segment 1560 includes a proximal articulation driver 1700 (see FIG. 7) that operably interfaces with a source of articulation and retraction as described in detail herein. The joint lock 1210 (FIG. 6) activated by 6) can be operably supported. In the example shown in FIG. 15A, end effector mounting assembly 1230 is pivotally attached to distal spine extension 1562 by distal support link 1570. In one mechanism, for example, the end effector mounting assembly 1230 is pinned to the distal end 1572 of the distal support link 1570 by an articulation pin 1580 that defines an articulation axis BB. Proximal end 1574 of distal support link 1570 is attached to distal end 1563 of distal spine extension 1562 and moves axially and pivotally therewith.

  As further seen in FIG. 15A, the proximal end 1574 of the distal support link 1570 is for slidably and pivotally receiving a proximal mounting pin 1578 mounted on the distal spine extension 1562 therein. And an axial slot 1576 sized. Such a mechanism allows the surgical end effector 1100 to selectively pivot about the articulation axis BB relative to the distal frame segment 1560 (articulation), and to provide some limited axial movement. And serves to couple to the distal frame segment 1560. In the mechanism shown, articulation is applied to the surgical end effector 1100 by a distal articulation link 1710 that is pivotally coupled to or otherwise operably interfaces with the articulation lock 1210. Axial movement of the distal articulation link 1710 in the proximal direction PD (constrained to move axially along one side of the shaft axis SA) causes the surgical end effector 1100 to move surgically. In the leftward LD from an unarticulated position where the end effector 1100 is axially aligned on the shaft axis SA to an articulated position on the left side of the shaft axis SA (represented by the phantom line in FIG. 15A). Articulate. Axial movement of the distal articulation link 1710 in the distal direction DD moves the surgical end effector 1100 from an articulated position to an inactive position (arrow RD). In one mechanism, when the surgical end effector 1100 reaches the inactive position, it contacts the distal end 1563 of the distal spine extension to prevent it from moving further in the right direction RD. A stop member or stop formation 1232 is formed in end effector mounting assembly 1230 or otherwise attached to end effector mounting assembly 1230. Such an articulation mechanism may provide improved articulation movement and closure stability.

  In addition to the above, the exchangeable surgical tool assembly 1000 further includes a clutch assembly 1640 that can be configured to selectively and releasably couple the proximal articulation driver 1700 to the firing member assembly 1600. . In one form, the clutch assembly 1640 includes, in at least one embodiment, a rotating lock assembly that includes a lock collar or lock sleeve 1650 positioned around the firing member assembly 1600. The locking sleeve 1650 includes an engagement position where the locking sleeve 1650 connects the proximal articulation driver 1700 to the firing member assembly 1600 and an engagement position where the proximal articulation driver 1700 is not operably connected to the firing member assembly 1600. It is configured to be rotated between the engagement release position. When locking sleeve 1650 is in its engaged position, distal movement of firing member assembly 1600 can cause proximal articulation driver 1700 to move distally, and correspondingly, firing member assembly 1600. Can move proximal articulation driver 1700 in the proximal direction. When the lock sleeve 1650 is in its disengaged position, movement of the firing member assembly 1600 is not transmitted to the proximal articulation driver 1700 so that the firing member assembly 1600 is independent of the proximal articulation driver 1700. Can be moved. Under various circumstances, the proximal articulation driver 1700 is held in place by the articulation lock 1210 when the proximal articulation driver 1700 is not moved proximally or distally by the firing member assembly 1600. Can be done.

  Referring primarily to FIGS. 4 and 5, locking sleeve 1650 is cylindrical, or at least substantially, including a longitudinal opening 1652 configured to receive a proximal firing shaft segment 1602 of firing member assembly 1600. Equipped with a cylindrical body. The locking sleeve 1650 also has two diametrically opposed, inward locking protrusions 1654 formed thereon and an outwardly directed second locking member 1656. Lock protrusion 1654 may be configured to selectively engage a proximal firing shaft segment 1602 of firing member assembly 1600. More specifically, when locking sleeve 1650 is in its engaged position, locking protrusion 1654 is positioned within drive notch 1603 provided within proximal firing shaft segment 1602, thereby providing a distal pushing force. And / or proximal pulling force may be transmitted from firing member assembly 1600 to locking sleeve 1650. When the locking sleeve 1650 is in its engaged position, the second locking member 1656 is received in a drive notch 1704 defined in the proximal articulation driver 1700, thereby providing a distal lock applied to the locking sleeve 1650. The pushing force and / or the proximal pulling force may be transmitted to the articulation driver 1700. In effect, firing member assembly 1600, locking sleeve 1650, and proximal articulation driver 1700 move together when locking sleeve 1650 is in its engaged position. On the other hand, when the locking sleeve 1650 is in its disengaged position, the locking protrusion 1654 cannot be positioned within the drive notch 1603 of the proximal firing shaft segment 1602 of the firing member assembly 1600, resulting in a distal Pushing and / or proximal pulling forces cannot be transmitted from firing member assembly 1600 to locking sleeve 1650. Correspondingly, the distal pushing force and / or the proximal pulling force cannot be transmitted to the proximal articulation driver 1700. Under such circumstances, firing member assembly 1600 may be slid proximally and / or distally with respect to locking sleeve 1650 and proximal articulation driver 1700.

  Clutch assembly 1640 further includes a switch drum 1630 that interfaces with locking sleeve 1650. Further details regarding the operation of switch drum 1630 and lock sleeve 1650 can be found in U.S. Patent Applications Nos. 13 / 803,086 and 15 / 019,196, each of which is incorporated herein by reference in its entirety. be able to. The switch drum 1630 can further include an at least partially circumferentially extending opening 1632 defined therein, the opening 1632 being a circumferential mounting portion extending from the nozzle portion 1302, 1304. Receiving 1305 may allow relative rotation between switch drum 1630 and proximal nozzle 1301 but not translation. Please refer to FIG. Rotation of the nozzle 1301 to the point where the mount reaches the end of these corresponding openings 1632 in the switch drum 1630 causes the switch drum 1630 to rotate about the shaft axis SA. Rotation of switch drum 1630 eventually results in movement of lock sleeve 1650 between its engaged and disengaged positions. In an alternative embodiment, nozzle 1301 may be used to operably engage and disengage an articulation drive system with a firing drive system. As indicated above, the clutch assembly 1640 can operate in various ways as described in further detail in U.S. Patent Applications Nos. 13 / 803,086 and 15 / 019,196.

  In the mechanism shown, the switch drum 1630 includes an L-shaped slot 1636 that extends into a distal opening 1637 of the switch drum 1630. The distal opening 1637 receives the lateral switch pin 1639 of the shifter plate 1638. In one embodiment, shifter plate 1638 includes a longitudinal slot (not shown) provided in lock sleeve 1650 to facilitate axial movement of lock sleeve 1650 when engaged with proximal articulation driver 1700. ) Is accepted within. For further details regarding the operation of the shifter plate and shift drum mechanism, see US Pat. SURGICAL STAPLING INSTRUMENT WITH SHAFT RELEASE, POWERED FIRING AND POWERED ARTICULATION.

  Also, in the illustrated embodiment, the switch drum 1630 includes a magnet support arm 1665 that supports a magnet or other sensor mechanism, wherein the magnet or other sensor mechanism is a slip ring assembly 1660 operably mounted on the chassis 1800. It is configured to operably interface with a Hall effect sensor 1662 that interfaces with the sensor. Slip ring assembly 1660 may, for example, conduct power and / or transfer signals to and from exchangeable surgical tool assembly 1000 and components of exchangeable surgical tool assembly 1000. And / or configured to communicate from the replaceable surgical tool assembly 1000 back to the microcontroller 520 (FIG. 2) or the robotic system controller in the handle assembly 500. Further details regarding the slip ring assembly 1660 and associated connectors are provided in U.S. Patent Applications Nos. 13 / 803,806 and 15 / 019,196, each of which is incorporated herein by reference in its entirety. No. 13 / 800,067, entitled "STAPLE CARTRIDGE TISSUE THICKNESS SENSOR SYSTEM", which is incorporated herein by reference in its entirety, (now US Patent Application Publication No. 2014/0263552). it can. The magnet (s) supported on the magnet support arm 1665, in cooperation with a Hall effect sensor 1662 or other sensor mechanism, detects the rotational position of the switch drum 1630 and transmits that information to the microcontroller 520. , Microcontroller 520 may serve to provide instructions (or instructions) to the user in various ways as described in the incorporated references above. Other sensor mechanisms may be used.

  Referring again to FIGS. 2 and 5, the chassis 1800 is formed on the chassis 1800 and adapted to be received in a corresponding dovetail slot 507 formed in the distal end portion of the frame 506 of the handle assembly 500. It also includes at least one, preferably two, tapered mounting portions 1802. As can be further seen in FIG. 2, a shaft mounting lug 1607 is formed at the proximal end of the proximal firing shaft segment 1602. As will be described in greater detail below, when the replaceable surgical tool assembly 1000 is coupled to the handle assembly 500, a shaft mounting lug 1607 is provided on the firing shaft formed at the distal end of the longitudinally movable drive member 540. It is received in the mounting cradle 542. Please refer to FIG.

  The replaceable surgical tool assembly 1000 uses a latch system 1810 for removably connecting the replaceable surgical tool assembly 1000 to the frame 506 of the handle assembly 500. As seen in FIG. 5, for example, in at least one form, the latch system 1810 includes a locking member or lock yoke 1812 movably coupled to the chassis 1800. In the illustrated embodiment, for example, the lock yoke 1812 is U-shaped and includes two downwardly extending legs 1814. Each of the legs 1814 has a pivot lug (not shown) formed thereon adapted to be received in a corresponding hole 1816 formed in the chassis 1800. Such a mechanism facilitates pivotally attaching the lock yoke 1812 to the chassis 1800. Lock yoke 1812 includes two proximally projecting lock lugs 1818 configured to releasably engage corresponding lock detents or grooves 509 in the distal end of frame 506 of handle assembly 500. May be. Please refer to FIG. In various forms, the lock yoke 1812 is biased proximally by a spring or biasing member 1819. Actuation of the lock yoke 1812 may be accomplished by a latch button 1820 slidably mounted on a latch actuator assembly 1822 mounted on the chassis 1800. Latch button 1820 may be biased proximally relative to lock yoke 1812. Lock yoke 1812 can be moved to an unlocked position by biasing latch button 1820 in a distal direction, which further causes lock yoke 1812 to pivot to the distal end of frame 506. Is disengaged in a retaining manner. When locking yoke 1812 is "retentively engaged" with the distal end of frame 506, locking lugs 1818 are seated resiliently in corresponding lock detents or grooves 509 in the distal end of frame 506. ing.

  In the mechanism shown, the locking yoke 1812 includes at least one, and preferably two, locking hooks 1824 adapted to contact corresponding locking lug portions 1426 formed on the closure shuttle 1420. When the closure shuttle 1420 is in the inoperative position, the locking yoke 1812 can be pivoted distally to unlock the replaceable surgical tool assembly 1000 from the handle assembly 500. When in this position, the lock hook 1824 does not contact the lock lug portion 1426 on the closure shuttle 1420. However, when the closure shuttle 1420 is moved to the operative position, the lock yoke 1812 is prevented from pivoting to the unlocked position. In other words, if the clinician attempts to pivot lock yoke 1812 to the unlocked position, or inadvertently, for example, lock yoke 1812 may be otherwise pivoted distally. , The lock hook 1824 on the lock yoke 1812 contacts the lock lug 1426 on the closure shuttle 1420 to prevent the lock yoke 1812 from moving to the unlocked position. Please refer to FIG. Further details regarding the latch system can be found in US Patent Application Publication No. 2014/0263541.

  The attachment of the replaceable surgical tool assembly 1000 to the handle assembly 500 will now be described with reference to FIG. To begin the connection process, the clinician may replace the chassis 1800 of the replaceable surgical tool assembly 1000 such that the tapered mounting portion 1802 formed on the chassis 1800 is aligned with the dovetail slot 507 of the frame 506. It may be located above or adjacent the distal end of frame 506. The clinician then moves the surgical tool assembly 1000 along the installation axis IA perpendicular to the shaft axis SA to move the tapered mounting portion 1802 into a corresponding dovetail receiving slot 507 at the distal end of the frame 506. The seat may be seated in an “operably engaged” state. In doing so, the shaft mounting lug 1606 on the proximal firing shaft segment 1602 is also housed in the cradle 542 of the longitudinally movable drive member 540, and a portion of the lateral mounting pin 516 on the closure link mechanism 514 is removed. , Seated in a corresponding hook 1421 of the closure shuttle 1420. As used herein, the term "operable engagement" in the context of two components means that when the two components are sufficiently engaged with each other, thereby applying an actuating movement, the components Can perform the intended action, function, and / or procedure.

  Referring again to FIGS. 11 and 15, the distal firing bar 1620 may include a stacked beam structure that includes at least two beam layers. Such beam layers may include, for example, stainless steel bands interconnected by welding or pinning together at their proximal ends and / or at other locations along their length. . In an alternative embodiment, the distal ends of the bands are not connected together to allow the stack or band to spread relative to each other as the end effector articulates. Such a mechanism allows the distal firing bar 1620 to be sufficiently flexible to accommodate the articulation of the end effector. Various other suitable laminated knife bar mechanisms are disclosed in U.S. Patent Application No. 15 / 019,245. As further seen in FIG. 4, central support member 1614 provides lateral support to distal firing bar 1620 as distal firing bar 1620 flexes to accommodate articulation of surgical end effector 1100. Used to bring. Further details regarding the center support member and the alternative knife bar support mechanism are disclosed in US patent application Ser. No. 15 / 019,245.

  After the replaceable surgical tool assembly 1000 is operatively connected to the handle assembly 500 (FIG. 1), the clinician can operate the surgical tool assembly 1000 as follows. As described above, when the closure drive system 510 is in its inactive position (ie, the closure trigger 512 is not activated), the torsion spring 1642 causes the clutch assembly 1640, and more specifically, the switch pin 1639 and the lock The sleeve 1650 is biased to the articulated position. When in this mode, the magnet (s) in the magnet support arm 1665 cooperate with the Hall effect sensor 1662 or other sensor mechanism to indicate that the surgical tool assembly 1000 is in the articulation mode. Can be shown. When the clinician activates firing trigger 532, the motor drives proximal firing shaft segment 1602 in a distal direction. However, as described above, the slip joint 1622 facilitates movement of the proximal firing shaft segment 1602 without, or at least substantially without, moving the distal firing bar 1620. Activation of the proximal firing shaft segment 1602 causes the proximal joint shaft segment 1602 to operatively engage the proximal firing shaft segment 1602 and the proximal articulation driver 1700 to engage the proximal firing shaft segment 1602 as the locking sleeve 1650 engages the locking sleeve 1650. Distal movement of the motion driver 1700 is provided. Distal movement of the proximal articulation driver 1700 causes the surgical end effector 1100 to articulate about the articulation axis BB. During this time, the clinician can further partially close the jaws of the surgical end effector 1100 by partially pressing the closure trigger. Such a mechanism facilitates axial movement of the proximal closure member 1410 without automatically shifting the clutch assembly 1640 to the firing mode. This feature may allow a clinician to use the jaws to grasp and manipulate tissue before clamping onto target tissue.

  When the clinician articulates the surgical end effector 1100 to the desired position and the jaws are positioned in the desired orientation with respect to the target tissue, the clinician releases the firing trigger 532, which causes the proximal firing shaft segment 1602 and The motor drive motion of the proximal joint motion driver 1700 is interrupted. The articulation lock 1210 locks the proximal articulation driver 1700 in that position to prevent further articulation of the surgical end effector 1100. The clinician can clamp the target tissue between the jaws by depressing the closure trigger 512 to the fully depressed position. Such movement causes proximal closure member 1410 to move distally. Such distal movement of proximal closure member 1410 causes shifter plate 1638 to rotate locking sleeve 1650 to a disengaged position with proximal firing shaft segment 1602. When in this position, lock projection 1654 disengages from drive notch 1603 in proximal firing shaft segment 1602. Accordingly, the proximal firing shaft segment 1602 can move axially without moving the locking sleeve 1650 and the proximal articulation driver 1700. When proximal closure member 1410 is moved distally to a fully activated position (by pressing closure trigger 512), proximal closure member 1410 and distal closure member 1430 move distally to jaw 1130. , 1102 is closed. When in this position, the closure drive system 510 within the handle assembly 500 can be locked and the clinician can release the closure trigger 512. Once the clutch assembly 1640 moves to this firing mode, magnets or other sensors in the magnet support arm 1665 or other portion communicate with the Hall effect sensor 1662 to indicate the position of the clutch assembly 1640 to the microcontroller 520.

  Microcontroller 520 provides the clinician with an indication of the position of distal firing bar 1620 as distal firing bar 1620 is advanced distally through target tissue clamped between the end effector jaws. Is also good. Once the distal firing bar 1620, and more specifically, the firing member or knife member attached to the distal firing bar 1620 has advanced to the full firing position, the microcontroller 520 uses a sensor mechanism to control the firing member assembly 1600. The position of the portion may be detected, and then the motor may be reversed to retract the distal firing bar 1620 to its starting position. This action may be automatic or the clinician may need to depress firing trigger 532 during the retreat process. Once the distal firing bar 1620 has been fully retracted to its starting position, the microcontroller 520 will have the distal firing bar 1620 fully retracted, unlock the closure trigger 512 and deactivate the closure assembly 1406. Back to the position, thereby providing an indication to the clinician that the jaws can be moved to the open position.

  In one embodiment, the elongate channel 1102 is generally C-shaped with two upstanding sidewall portions 1104. Anvil 1130 includes an anvil body 1132 and an anvil mounting portion 1134. Anvil mounting portion 1134 includes a pair of anvil mounting walls 1136 separated by slots 1138 (FIG. 6). As described above, the end effector mounting assembly 1230 extends through a lateral mounting hole 1231 in the end effector mounting assembly 1230 and is received in a channel mounting hole 1106 provided in a sidewall 1104 of the elongated channel 1102. Attached to the proximal end 1103 of the elongate channel 1102 by a spring pin connector 1235 provided. Each anvil mounting wall 1136 has an anvil trunnion 1137 projecting therefrom, such that each anvil trunnion 1137 is rotatably received in a corresponding anvil mounting hole 1107 in the proximal end 1103 of the elongated channel 1102. Have been adapted. As seen in FIGS. 16 and 17, each of the channel sidewall portions 1104 may have a vertical slot or released area 1108 corresponding to each anvil mounting hole 1107, wherein the vertical slot or released area 1108 is Allows anvil trunnions 1137 to fall vertically into each slot 1108 for ease of assembly. The anvil trunnion defines a pivot axis PA about which the anvil 1130 is selectively pivotable with respect to the elongate channel 1102. In various embodiments, the pivot axis PA traverses the shaft axis SA. See FIG.

  Elongate channel 1102 is configured to operatively support surgical staple cartridge 1150 therein. The surgical staple cartridge 1150 includes a cartridge body 1151 that defines a deck surface 1152 facing the staple forming lower surface 1133 of the anvil body 1132. The cartridge body 1151 has an elongated slot 1154 extending through the cartridge body 1151 to allow passage of a firing member 1670 attached to the distal end of the distal firing bar 1620. The cartridge body 1151 has a plurality of anvil pockets 1156 linearly arranged in series on both sides of an elongated slot 1154. Please refer to FIG. A staple driver operably supporting one or more surgical staples or fasteners thereon is housed in these pockets 1156. When the target tissue is clamped between the staple forming lower surface 1133 of the anvil body 1132 and the staple cartridge deck surface 1152, the target tissue is positioned such that the tissue to be cut is stapled on each side of the cutting line. It is necessary to. The anvil 1130 may include two downwardly extending tissue stops 1140 to prevent the target tissue from being located proximal to the most proximal staple or fastener. See FIG. The tissue stop 1140, when extending down beyond the cartridge deck surface 1152, serves to prevent target tissue from reaching excessive proximal between the anvil 1130 and the surgical staple cartridge 1150.

  18 and 19, in the illustrated embodiment, the anvil mounting wall 1136 is somewhat elongated and extends in a proximal direction. In one embodiment, one or both of the anvil mounting walls 1136 includes an aperture limiter 1139 (FIG. 18) formed thereon, which contacts the end effector mounting assembly 1230 to contact the anvil 1130. Is configured to prevent excessive opening. See FIG. Such an anvil opening limiter 1139 can prevent the anvil 1130 from becoming too loose on the elongated channel 1102 and loose. In addition, the aperture limiter 1139 prevents the anvil 1130 from opening to a position where the tissue stop 1140 extends above the cartridge deck surface 1152. When this occurs, tissue may be able to extend too proximally between the anvil 1130 and the surgical staple cartridge 1150, and may be cut but not stapled. is there. Such a mechanism may also serve to prevent the anvil from being perceived as too loose and untight relative to the elongated channel.

  Referring again to FIG. 17, the anvil mounting portion 1134 defines a firing member “parking area” 1141 that houses the firing member 1670 when the firing member 1670 is in the start (unfired) position. In the illustrated mechanism, at least a portion of the parking area 1141 is proximal to the pivot axis. For example, see FIG. Such a mechanism may reduce negative moment arms arising from tissue clamped between the anvil 1130 and the surgical staple cartridge 1150 supported within the elongate channel 1102. In one embodiment, an anvil cap or cover 1142 is attached to anvil mounting portion 1134 and closed for contact by a distal camming ramp or surface 1440 formed on distal end 1431 of distal closure member 1430. A front surface 1143 is provided. See FIG. In one arrangement, anvil cap 1142 includes a pair of downwardly extending legs 1144 configured to snap into engagement with mounting lugs 1145 formed on anvil mounting wall 1136. As seen in FIG. 16, for example, an anvil cap 1142 extends between the anvil mounting walls 1136 and extends distally to cover the firing member 1670 when it is within the firing member retention area 1141. Existing transition portion 1146. Transition portion 1146 extends between anvil mounting wall 1136 and forms a transition from anterior closure surface 1143 and anvil cam surface 1147 formed on anvil mounting portion 1134. In addition, the anvil cap 1142 provides a pinch point that could otherwise exist between the anvil mounting portion 1134 and the distal end 1431 of the distal closure member 1430 when the anvil 1130 was in its fully open position. Can be minimized.

  Here, the operation of the closing process used in this embodiment will be described with reference to FIGS. 18A, 19, and 20A. In the mechanism shown, anvil body 1132 defines an upper anvil surface 1135. As seen in FIG. 18A, the cam area or cam surface 1147 formed on the anvil mounting portion 1134 gradually transitions to the upper anvil surface 1135. More specifically, in the illustrated mechanism, the cam surface 1147 comprises two surface portions, a proximal cam surface portion 1147P and a distal cam surface portion 1147D. In at least one example, proximal cam surface portion 1147P extends from the proximal end of anvil body 1132 to distal cam surface portion 1147D. Distal cam surface portion 1147D extends from proximal cam surface portion 1147P to upper anvil surface 1135. In one arrangement, the proximal cam surface portion 1147P may have a slightly steeper angle than the distal cam surface portion 1147D. In other arrangements, the cam surface on the anvil mounting portion may comprise one continuous cam surface oriented at a single cam angle with respect to the outer surface.

  As seen in FIG. 19, the distal closure member 1430 has a distal end surface 1431 formed on its distal end. Distal camming surface 1440 extends at an obtuse cam angle CA with respect to distal end surface 1431. In the mechanism shown, the distal closure member 1430 comprises a distal closure tube having an outer surface 1433 and an inner surface 1435 defining a cross-sectional thickness CT. The distal end surface 1431 includes a portion of the cross-sectional thickness CT. Distal camming surface 1440 extends from distal end surface 1431 of distal closure member 1430 to inner surface 1435. Initial cam area 1437 includes the intersection or intersection between distal end surface 1431 and distal camming surface 1440.

  FIG. 18A shows distal closure member 1430 in a starting position with anvil 1130 in an open position. As seen in FIG. 18A, the distal camming surface 1440 is in contact with the anterior closure surface 1143 on the anvil cap 1142. To begin the closing process, distal closure member 1430 is advanced axially in distal direction DD. When the initial cam area 1437 and / or the distal end surface 1431 first contact the cam surface 1147 (the proximal cam surface portion 1147P), an initial closing motion or force ICF is applied thereto. See FIG. This initial closing force ICF is perpendicular or perpendicular to the proximal cam surface portion 1147P. Continued axial advancement of the distal closure member 1430 causes the distal camming surface 1440 to come into engagement with the cam surface 1147 (distal cam surface 1147D) and exerts a closing force CF essentially parallel to the shaft axis SA. Add essentially. See FIG. 20A.

  In the above embodiment, the anvil mounting wall 1136 may have a somewhat longer length than the anvil mounting configuration used by other anvil mechanisms. The elongated anvil mounting wall 1136 thus serves to allow the pivot axis to be located relatively close to the articulation axis defined by the articulation 1200. This mechanism facilitates the establishment of a longer initial moment arm MAI (FIG. 19) between the pivot axis PA and the initial closing force ICF. Such a mechanism also facilitates the location of the pivot axis PA to be slightly closer to the bottom of the elongate channel 1102 compared to other anvil / channel mounting mechanisms. Thus, in the illustrated mechanism, the distance between the pivot axis PA and the axis on which the closing force CF is applied is somewhat larger than the other mechanisms (larger moment arms). This mechanism may also result in establishing a greater closing force CF as compared to other anvil mounting mechanisms. Thus, the anvil mounting mechanism of the illustrated embodiment can provide a greater mechanical closure effect than is generally achievable with other anvil mounting mechanisms. Another advantage that may be obtained by the foregoing example is that placing at least a portion of the firing member parking area 1141 proximal to the pivot axis PA is added to the anvil by tissue clamped between the anvil and the cartridge. What can help reduce the "negative" moment arm.

  Referring now to FIGS. 21-25, the distal closure member 1430 is formed with at least one, and preferably two, positive jaw opening hooks or tabs 1442. Tab 1442 may also be referred to herein as a "primary positive jaw opening tab." In one embodiment, the positive jaw opening tab is formed integrally with the distal closure member 1430. For example, a positive jaw opening tab 1442 is cut from the wall of the tubular structure that includes the distal closure member 1430. Each of the positive jaw opening tabs 1442 includes an upwardly projecting hook portion 1444 having a rounded camming end 1445 formed thereon, wherein the camming end 1445 extends downwardly from the anvil body 1132. An extended, corresponding anvil opening ramp 1148 is configured to come into engagement. FIG. 22 shows the position of anvil 1130 and distal closure member 1430 when anvil 1130 is in a closed orientation. FIG. 23 shows the start of the opening process, with the distal closure member 1430 beginning to retract in the proximal direction PD. As seen in FIG. 23, the camming end 1445 is initially in contact with the anvil opening ramp 1148. FIG. 24 shows the anvil 1130 in a partially open position, and FIG. 25 shows the anvil 1130 in a fully open position. As can be seen in FIG. 25, the camming end 1445 is on the bottom end 1149 of the anvil opening ramp and holds the anvil 1130 in a fully open position. Using such a feature on the distal closure member to achieve opening of the anvil from a fully closed position to a fully open position may be referred to herein as a "normal jaw opening" feature. Another suitable positive jaw opening mechanism is disclosed in U.S. Patent Application No. 14 / 742,925, entitled "SURGICAL END EFFECTORS WITH POSITIVE JAW OPENING ARRANGEMENTS," which is incorporated herein by reference in its entirety. ing.

  FIGS. 26-29 illustrate an alternative distal closure member 1430 ′ using a secondary positive jaw opening tab 1448 configured to cooperate with a secondary jaw opening feature 1160 formed on the anvil mounting wall 1136. Is shown. Please refer to FIG. 16, FIG. 17, and FIG. As seen in FIG. 26, the secondary positive jaw opening tab 1448 contacts the secondary jaw opening feature 1160 on the anvil 1130 as the distal occlusion tube or member 1430 'is moved in the proximal direction PD. Can be cut into the wall of the distal occlusion tube or member 1430 'and folded inward. FIG. 29 shows the anvil 1130 in the fully open position. As the distal closure member 1430 'is moved proximally, the primary positive jaw opening tab 1442 cams up the corresponding anvil opening ramp 1148 on the anvil 1130 to pivot the anvil. And let it open. Thereafter, during the closing process, the secondary positive jaw opening tab 1448 in the distal closure member 1430 ′ contacts the secondary jaw opening feature 1160 formed on the anvil mounting wall 1136 to move the anvil 1130 to the fully open position. Further assistance in moving to. As seen in FIG. 26, the secondary positive jaw opening tab 1448 generally follows the contour of the distal closure tube 1430 '.

  FIG. 30 shows an alternative distal closure member 1430 ', where the secondary positive jaw opening tab 1448 is formed integrally with the wall of the distal closure tube 1430', but with the distal closure tube or The member 1430 'extends proximally inward so as to contact the secondary jaw opening feature 1160 on the anvil 1130 when moved in the proximal direction PD. FIG. 31 shows the anvil 1130 in a fully open position. Accordingly, such primary and secondary anvil openings or jaw opening features may be opened to the anvil when the distal closure member moves from a fully activated position corresponding to the fully closed position of the anvil to a non-activated position corresponding to the fully opened position of the anvil. It may function to add exercise sequentially. In such a mechanism, when the distal closure tube 1430 'is moved in a proximal direction, the primary positive jaw opening tab 1442 cams the anvil into a "substantially open" position. Secondary positive jaw opening tab 1448 functions to ensure that the anvil is moved to its fully open position when the distal closure member returns to the inactive position.

  32 and 33 illustrate an alternative secondary anvil extension 1162 in which anvil mounting wall 1136 includes a proximal anvil extension 1162 that cooperates with a corresponding secondary anvil biasing spring 1164 to bias the anvil to an open position. 3 shows a forward jaw opening mechanism. As the distal closure member 1430 is moved in a proximal direction, the primary positive jaw opening tab 1442 cams up to the corresponding anvil opening ramp 1148 on the anvil 1130 and begins to pivot and open the anvil. In addition, secondary anvil biasing spring 1164 applies a biasing force on proximal anvil extension 1162 to further assist in moving anvil 1130 to a fully open position. In conventional jaw opening mechanisms, there is a "lag time" between the actuation of the jaw opening system (e.g., a firing trigger) and the ongoing opening of the jaw. In the embodiment described above, the secondary anvil biasing spring 1164 is located proximal to the pivot axis PA about which the anvil pivots relative to the elongated channel. Such a mechanism not only increases the biasing (opening) movement to the anvil, but in other cases, the initial retraction of the closure member and the closure member applies a sufficient amount of opening movement to the anvil to cause the anvil to move. It may function to minimize the occurrence of any "dead zone" that may occur between the point where it actually begins to move to the open position.

  FIGS. 34 and 35 show an alternative distal closure member 1430 ″ using a positive jaw biasing member 1450 over each of the positive jaw opening tabs 1442. Positive jaw biasing member 1450 may form a leaf-type spring mechanism formed of metal or the like, and an anvil opening ramp on anvil 1130 when distal closure member 1430 ″ is moved in a proximal direction PD. It acts to apply an additional opening force to 1148. FIG. 34 shows the anvil 1130 in a fully closed position, and FIG. 35 shows the anvil 1130 in a fully open position. FIGS. 36 and 37 show an alternative distal closure member 1430 ″ using another form of positive jaw biasing member 1452 on each of the positive jaw opening tabs 1442. The positive jaw biasing member 1452 may have a somewhat V-shaped configuration, and may be formed from spring steel or the like. FIG. 36 shows the anvil 1130 in a fully closed position, and FIG. 37 shows the anvil 1130 in a partially open position as the distal closure member 1430 ″ first moves proximally. Positive jaw biasing member 1452 functions to ensure that anvil 1130 is lifted relative to distal closure member 1430 '' from the start of the opening process.

  FIGS. 38 and 39 illustrate an alternative distal closure member 1430 '', wherein the positive jaw opening tabs 1442, respectively, are raised relative to the distal closure member 1430 '' from the start of the opening process of the anvil 1130. Has a flexible portion 1454 that functions to ensure that Flexible portion 1454 may include rubber or a similar material formed on hook portion 1444 of positive jaw opening tab 1442. In other arrangements, portion 1454 may not be formed from a compliant material, but may instead be formed from a hardened material to prevent wear on positive jaw opening tab 1442. FIG. 38 shows the anvil 1130 in a fully closed position, and FIG. 39 shows the anvil 1130 in a partially open position. Such a flexible mechanism and biasing member mechanism bias the anvil to open while the closing member cam mechanism remains in camming engagement with the cam ramp on the anvil to actuate the closing system (the anvil). And to function to minimize any dead zone lag that occurs between the anvil and the actual opening of the anvil. Such an arrangement may also serve to establish a solid camming surface that allows the user to override the anvil jam by manipulating the closure trigger.

  40-42, the firing member 1670 is configured to operably interface with a sled or cam assembly 1120 operably supported within the body 1151 of the surgical staple cartridge 1150. The cam assembly 1120 is slidably displaceable within the surgical staple cartridge body 1151 from a proximal start position adjacent the proximal end 1153 of the cartridge body 1151 to an end position adjacent the distal end 1155 of the cartridge body 1151. It is. The cartridge body 1151 operably supports a plurality of staple drivers (not shown) aligned in rows on each side of a centrally located slot 1154. The centrally located slot 1154 allows the firing member 1670 to pass therethrough and cut tissue clamped between the anvil 1130 and the surgical staple cartridge 1150. The driver is associated with a corresponding pocket 1156 that opens through the upper deck surface 1152 of the cartridge body 1151. The staple drivers each support one or more surgical staples or fasteners (not shown) thereon. Accordingly, a plurality of surgical staples are arranged in lines or rows located on opposite sides of slot 1154. Cam assembly 1120 includes a plurality of angled or wedge-shaped cams 1122, each cam 1122 corresponding to a particular line of fasteners or drivers located on the side of slot 1154. When firing member 1670 is fired or driven distally, firing member 1670 also drives cam assembly 1120 in a distal direction. As firing member 1670 moves distally through surgical staple cartridge 1150, tissue cutting mechanism 1676 cuts tissue clamped between anvil 1130 and surgical staple cartridge 1150, and cam assembly 1120 moves into the cartridge. Drives the driver upwards, which drives the corresponding staples or fasteners to form contact with the anvil 1130.

  In those embodiments where the firing member includes a tissue cutting surface or tissue cutting mechanism, the firing member may be incorrect unless the unfired or new staple cartridge is properly supported within the elongated channel 1102 of the surgical end effector 1100. It may be desirable to configure the elongate shaft assembly in such a way as to prevent advancement. For example, if there is no staple cartridge and the firing member is advanced distally through the end effector, the tissue will be cut but not stapled. Similarly, if a used staple cartridge (i.e., a staple cartridge from which at least some of the staples have already been fired) is present in the end effector and the firing member is advanced, tissue may be severed. However, stapling may not be complete, if at all. It will be apparent that the occurrence of such a phenomenon can lead to undesirable catastrophic consequences during the surgical procedure. U.S. Pat. No. 6,988,649, title of the invention "SURGICAL STAPLING INSTRUGING SPACE INFORMATION PRODUCT INFORMATION WORKING SPACE INFORMATION CONFIGURATION And U.S. Patent No. 7,380,695; title of invention "SURGICAL STAPLING INSTRUMENT HAVING A SINGLE LOCKOUT MECHANISM FOR PREVENTION OF FIRING"; and U.S. Patent Application No. 14 / 742,933; AL STAPLING INSTRUMENTS WITH LOCKOUT ARRANGEMENTS FOR PREVENTING FIRING SYSTEM ACTUATION WHEN A CARTRIDGE IS SPENT OR MISSING " Each of these references is incorporated herein by reference in its entirety.

  An “unfired”, “unused”, “new”, or “new” surgical staple cartridge 1150, as used herein, means that the surgical staple cartridge 1150 has been properly loaded into an end effector. Sometimes it means having all of the fasteners in their "firing" position. When in that position, cam assembly 1120 is in its starting position. A new surgical staple cartridge 1150 can be seated within the elongate channel 1102 and retained therein by a snap mechanism on the cartridge body configured to resiliently engage a corresponding portion of the elongate channel 1102. FIG. 41 shows a portion of a surgical end effector 1100 with a new or unfired surgical staple cartridge 1150 seated therein. As seen in FIG. 41, the cam assembly 1120 is in a starting position. More precisely, to prevent the firing system from being actuated, the firing member 1670 is moved farther through the end effector 1100 unless an unfired or new surgical staple cartridge is properly seated in the elongated channel 1102. To prevent lateral movement, the illustrated replaceable surgical tool assembly 1000 employs a firing member lockout system, generally designated as 1730, which, in certain aspects, is disclosed throughout its disclosure. No. 15 / 385,958, filed Dec. 21, 2016, entitled "SURGICAL INSTRUMENTS WITH LOCK LOCK ARRANGEMENTS FOR PREVENTING FIRING SYSTEM ACTUA, filed Dec. 21, 2016, which is hereby incorporated by reference herein. It can be similar to ION UNLESS AN UNSPENT STAPLE CARTRIDGE lockout systems disclosed IS PRESENT ".

  In the illustrated example, firing member lockout system 1730 is configured to engage resiliently with firing member 1670 when unused or unfired surgical staple cartridge 1150 is not properly seated in elongate channel 1102. Includes a configured movable lock member 1732. Locking member 1732 includes a pair of lateral spring arms 1733 interconnected by a central mounting tab mechanism 1734. As seen in FIG. 41, each of the lateral spring arms 1733 is laterally offset from the shaft axis SA. When the lock member 1732 is installed, the mounting tab mechanism 1734 is configured to urge the lock member 1732 upward. Additionally, locking member 1732 may be angled upward such that when anvil 1130 is closed, it engages the bottom surface of a corresponding anvil mounting wall 1136 on anvil mounting portion 1134 to urge locking member 1732 downward. And two lateral anvil spring arms 1736 forming the same. The distal portion of each lateral spring arm 1733 terminates in a sled tab 1738, each further laterally offset from the shaft axis SA. Each of the thread tabs 1738 is oriented to contact a corresponding unlocking mechanism or thread boss 1124 formed on the proximal end portion 1121 of the cam assembly 1120. As seen in FIG. 40, for example, in the illustrated mechanism, the cam assembly 1120 has a central axis CA. When the sled assembly 1120 is in its starting position in an unfired staple cartridge properly supported in the elongate channel, the central axis CA is laterally aligned with the shaft axis SA. As seen in FIG. 40, the thread boss is laterally offset from the central axis CA (and ultimately the shaft axis SA) to define a central region 1123 therebetween. As the firing member is advanced distally through the end effector, the firing member contacts the cam assembly 1120 in the central region to drive the cam assembly 1120 distally through the cartridge body. In an alternative mechanism, only one lateral spring arm 1733 may be used, and thus only one lateral thread tab 1738 is provided. In such a mechanism, only one corresponding thread boss 1124 is formed on the cam assembly 1120. In still other mechanisms, the locking member 1732 may have two lateral spring arms 1733, but only one of the lateral spring arms may have a thread tab 1738. In the illustrated mechanism, each of the proximally facing threaded bosses 1124 is for facilitating an easier interface between the threaded boss 1124 and the transverse threaded tab 1738 during placement of the cartridge in the elongated channel. Includes an inclined surface 1127.

  Each of the lateral spring arms 1733 includes a lock notch therein configured to lock with a corresponding central locking lug 1674 extending laterally from the firing member body portion 1672. FIG. 41 shows the cam assembly 1120 in the starting position with the thread boss 1124 lifting the locking member 1732 out of lock engagement with the locking lug 1674. FIG. 42 shows an incorrect surgical staple cartridge 1150W installed in connection with the locking member 1732. As seen in FIG. 42, the cartridge 1150W has a cam assembly 1120W having a proximally extending mechanism 1124W laterally offset from the center axis of the cam assembly, while the mechanism 1124W includes: The lock member 1732 is not in the lock release engagement state with the thread tab 1738. Therefore, even in the start position, the cam assembly 1120W does not move the lock member 1732 to be disengaged from the lock engagement with the firing member 1670.

  In an alternative mechanism, the locking member completes the electrical circuit when depressed and contacts the corresponding portion of the properly loaded unfired cartridge sled (when the sled is in its proper firing position). May be configured. In such a mechanism, for example, the motor is inoperable when the circuit is open. In one mechanism, the locking member can also mechanically engage the firing member in the manner described above, thereby facilitating both mechanical and electrical lockout mechanisms / functions.

  43-50 illustrate another firing member lockout system 1740 that may be used in connection with the various end effector embodiments disclosed herein. In this embodiment, firing member lockout system 1740 includes a locked position in which firing member lock 1742 locks with firing member 1670 and a free and distal movement of firing member 1670 through surgical staple cartridge 1150. Includes a firing member lock 1742 supported for pivotal movement between an advancing unlocked position. As seen in FIG. 43, the firing member lock 1742 includes a mounting portion 1743 having a pivoting member 1744 projecting laterally from each side thereof. Pivot member 1744 is pivotally captured within a pivot notch 1238 located below end effector mounting assembly 1230. See FIG. As seen in FIG. 44, pivot member 1744 is rotatably captured within pivot notch 1238 by lower dual pivot link 1222. As further seen in FIG. 43, a pair of hook arms 1746 extend distally from the mounting portion 1743. Each hook arm 1746 includes a lock notch 1748 formed thereunder configured to engage a corresponding one of the central locking lugs 1674 on the firing member 1670. The firing member lockout system 1740 includes a pair of biasing members in the form of a leaf spring or the like that engages a corresponding anvil mounting wall 1136 on the anvil 1130 and the firing member lock 1742 to bias the firing member lock 1742 downward. 1749.

  FIG. 45 illustrates the surgical end effector 1100 with the anvil 1130 and the elongate channel 1102 in a fully open position that occurs while loading an unused or unfired surgical staple cartridge 1150 therein. When in the open position, firing member 1670 cannot be advanced distally due to at least a misalignment of a portion of the firing member with a corresponding passage in anvil 1130. In addition, the device is configured to detect the position of the anvil and / or the configuration of other parts of the anvil closure system to prevent actuation of the firing system components unless the anvil is in the fully closed position. Various sensor mechanisms can be employed. As seen in FIG. 45, when in the open position, the hook arms 1746 are oriented in the inoperative position, where a portion of each of the hook arms 1746 is received on a corresponding central locking lug 1674 of the firing member 1670, As a result, the lock notch 1748 is not in a position to engage the corresponding central locking lug 1674.

  FIG. 46 shows the end effector after an unfired surgical staple cartridge 1150 with a sled or cam assembly 1120 has been properly installed in the elongate channel 1102 and the anvil 1130 has been closed. When in such a configuration, the biasing member 1749 exerts a downward biasing motion on the firing member lock 1742, where the firing member lock 1742 includes a threaded boss 1124 and a central locking lug 1674 on the firing member 1670. In contact. As further seen in FIG. 46, the thread boss 1124 on the thread assembly 1120 raises the firing member lock 1742 upwardly, thereby causing the locking notch 148 therein to engage with the central locking lug 1674 on the firing member 1670. It plays a role in removing it from the match. Accordingly, firing member 1670 is free to advance distally, as shown in FIG. As seen in FIG. 47, firing member lock 1742 is out of engagement with firing member 1670 and sled assembly 1120, and biasing member 1749 pivots firing member lock 1742 downward.

  48 to 50 show the retreat of the firing member 1670. FIG. 48 shows the position of firing member 1670 and firing member lock 1742 at the beginning of the retraction process. FIG. 49 shows the firing member after the tapered proximal end 1675 of the central locking lug 1674 contacts the angled surface on the distal end of the hook arm 1746 and pivots the hook arm 1746 upward (arrow U). 1670 is shown. FIG. 50 shows the firing member 1670 in its fully retracted or starting position. As seen in FIG. 50, hook arm 1746 has pivoted downward to a "pre-locked" position. When the locking member is in the pre-locked position, the firing member 1670 is locked with the hook harms 1746 on which the central locking lug 1674 serves to prevent further distal advancement of the firing member 1670. It can be moved distally until it engages. Thus, in the illustrated example, the firing member lock 1742 is not moved from the unlocked or inactive position to the active position unless the anvil is first moved to the closed position. In this context, the term "closed position" refers to a firing member lockout system where the anvil can be advanced distally relative to the cartridge and the firing member, in other cases, for example, internally. Is moved to a position where it cannot be advanced distally.

  51-55 illustrate another firing member lockout system 1750 that may be used in connection with various end effector embodiments disclosed herein. In this embodiment, the firing member lockout system 1750 includes at least one firing member lock 1752 supported for vertical movement along a lock axis LA transverse to the shaft axis SA. In one example, firing member locks 1752 correspond to each of anvil mounting walls 1136. In another example, only one firing member lock 1752 may be used. For clarity, only one firing member lock 1752 is shown in the figure. In the example shown, each firing member lock 1752 has an L-shape and a latch portion 1754. The firing member lock 1752 is movably supported on a corresponding mounting rod 1751 mounted on the corresponding anvil mounting wall 1136 or other portion of the anvil. The corresponding lock spring or biasing member 1756 biases the firing member lock 1752 downward (arrow D in FIGS. 52 and 53). FIG. 51 shows a surgical end effector 1100 with an anvil 1130 and an elongated channel 1102 in their fully closed position, with an unused or unfired surgical staple cartridge 1150 properly supported therein. As seen in FIG. 51, each tapered end 1755 of latch portion 1754 is engaged by a corresponding unlocking mechanism 1125 on sled assembly 1120. The unlocking mechanism 1125 serves to vertically shift the latch portion 1754 so that the central locking lug 1674 on the firing member 1670 can pass thereunder. Thus, firing member 1670 is free to advance distally. FIG. 52 illustrates the position of firing member 1670 at the beginning of the firing process, with firing member 1670 advanced distally from its starting position. As seen in FIG. 52, the unlock mechanism 1125 is no longer in contact with the latch portion 1754.

  53 to 55 show the retreat of the firing member 1670. FIG. 53 shows the position of firing member 1670 and firing member lock 1752 at the beginning of the retraction process. FIG. 54 shows that the tapered proximal end 1675 of the central locking lug 1674 contacts the angled surface or tapered end 1755 of the latch portion 1754 and has shifted the firing member lock 1752 vertically upward (FIGS. 54 and 55). Shows the position of firing member 1670 after arrow U). FIG. 55 shows the firing member 1670 in its fully retracted or starting position. As seen in FIG. 55, the firing member lock 1752 is in the locked or bottom position, and when the firing member 1670 is moved in a distal direction, the central locking lug 1674 on the firing member 1670 will have a corresponding firing. It contacts the latch portion 1754 of the member lock 1752. When in that position, firing member 1670 cannot advance distally. Since the firing member lock 1752 is mounted on the anvil, when the anvil is in the open position, the firing member lock 1752 is not in the locked position, which can prevent the firing member 1670 from advancing in the axial direction. Accordingly, to activate firing member lockout system 1750, anvil 1130 must first be moved to the closed position. In this context, the term "closed position" refers to a firing member lockout system where the anvil can be advanced distally relative to the cartridge and the firing member, in other cases, for example, internally. Is moved to a position where it cannot be advanced distally.

  FIGS. 56-63 illustrate another firing member that includes a movable locking member 1762 configured to resiliently engage firing member 1670 when surgical staple cartridge 1150 is not properly seated in elongate channel 1102. Shown is a lockout system 1760. Locking member 1762 is configured to at least one laterally configured to resiliently engage a corresponding portion of the firing member when sled assembly 1120 is not present within surgical staple cartridge 1150 in its starting position. A moving locking portion 1764 is provided. In the mechanism shown, the locking member 1762 employs two laterally moving locking portions 1764, each locking portion 1764 engaging a laterally extending portion of the firing member 1670.

  In the illustrated embodiment, the locking member 1762 comprises a generally U-shaped spring member, and each laterally movable leg or locking portion 1764 extends from the central spring portion 1763, FIGS. 56, 59, and It is configured to move in the lateral direction represented by the arrow “L” in 62. It will be understood that the term "lateral" refers to a direction transverse to the shaft axis SA. The spring or locking member 1762 may be made from high strength spring steel or a similar material. The central spring portion 1763 may include a proximally extending spring tab 1767 held in a notch 1240 in the end effector mounting assembly 1230. See FIG. In the illustrated example, the spring tab 1767 functions to bias the locking member 1762 to the unlocked configuration when the anvil 1130 is in the open position. FIG. 57 shows the anvil 1130 in an open position, ready for unfired or new cartridges to be installed in the elongate channel 1102. As can be seen in FIG. 57, the mounting tab 1767 urges the locking member 1762 in the upward direction (arrow U). When in its unlocked position, locking member 1762 is not in a position to prevent distal advancement of firing member 1762. However, the instrument can use other sensors and lockout mechanisms to detect the position of the anvil and otherwise prevent activation of the firing system unless the anvil has been moved to a closed position.

  FIG. 58 shows a portion of the surgical end effector 1100 after the unfired staple cartridge 1150 has been loaded or suitably supported within the elongate channel 1102 and the anvil 1130 has been moved to the closed position. . When the anvil 1130 is moved to the closed position, the anvil mounting wall 1136 contacts a corresponding laterally extending anvil tab 1766 formed on the locking member 1762. See FIG. Thus, the anvil mounting wall 1136 serves to move the lock member 1762 from the disengaged position to the locked position, where the lock member 1762 is in lock engagement with the firing member 1670. In one embodiment, each laterally movable leg or locking portion 1764 of locking member 1762 includes a locking window 1768 therein. When the locking member 1762 is in the locked position, a central locking lug 1674 on each side of the firing member 1670 extends into a corresponding locking window 1768 to allow the firing member 1670 to advance axially distally. To prevent retention.

  As seen in FIG. 56, the sled or cam assembly 1120 includes an unlocking mechanism 1125 corresponding to each of the laterally movable locking portions 1764. In the mechanism shown, an unlocking mechanism 1125 is provided on or extends proximally from each of the central wedge-shaped cams 1122. In an alternative mechanism, the unlocking mechanism 1125 may include a proximally projecting portion of a corresponding wedge-shaped cam 1122. As seen in FIG. 59, when the sled assembly 1120 is in its starting position, the unlocking mechanism 1125 engages the corresponding locking portion 1764 and corresponds to a direction transverse to the shaft axis SA (arrow L). The locking portion 1764 is biased laterally. When the locking portions 1764 are in these unlocked orientations, the central locking lugs 1674 are not in fixed engagement with their corresponding locking windows 1768. When in these orientations, the firing member 1670 may be advanced (firing) axially in a distal direction. However, if the unfired surgical staple cartridge 1150 is not present in the elongate channel 1102, or if the sled assembly 1120 has been moved out of its starting position (this is because the cartridge is at least partially or completely fired). Lock portion 1764 bounces laterally to resiliently engage firing member 1670. When in the position shown in FIG. 58, central locking lugs 1674 are received in their corresponding locking windows 1768 and are prevented from moving distally by lockout stops 1769. When in such a position, firing member 1670 cannot move distally.

  FIG. 61 shows the firing member 1670 when retracted to its start position or unfired position. When the tapered or tapered proximal end 1675 of the central locking lug 1674 contacts the radiused distal end 1765 of the movable locking portion 1764, the movable locking portion 1764 is moved, as shown in FIG. Each of the 1674 is urged laterally outward until it is completely received again in the lock window portion 1768 of the lock portion 1764 (FIG. 63). When firing member 1670 is fully retracted to the starting position shown in FIG. 63, firing member 1670 is re-locked in place by locking member 1762 and another new cartridge is properly inserted into elongated channel 1102 as described above. Is prevented from advancing distally until it is loaded. When the anvil 1130 is released, the spring tab 1767 re-biases the locking member 1762 to return to the unlocked or pre-actuated position. Accordingly, to activate firing member lockout system 1760, the user must first move the anvil to the closed position. In this context, the term "closed position" refers to a firing member lockout system where the anvil can be advanced distally relative to the cartridge and the firing member, in other cases, for example, internally. Is moved to a position where it cannot be advanced distally.

  FIGS. 64-70 illustrate an alternative joint locking mechanism 1910 for locking the surgical end effector 1100 'in a position articulated about a shaft axis SA about the articulation axis BB. In the illustrated example, the surgical end effector 1100 'is pivotally connected to the spine assembly 1500'. Spine assembly 1500 'may be attached to chassis 1800 (FIG. 4) in the manner described above. The distal end portion 1540 of the spine assembly 1500 'is formed with a downwardly projecting articulation pin 1542 defining an articulation axis BB. Articulating pin 1542 is configured to be rotatably or pivotally received within a spine mounting hole 1254 provided in mounting base 1252 of end effector mounting assembly 1250. End effector mounting assembly 1250 extends through lateral mounting hole 1251 of mounting assembly 1250 and is received in a channel mounting hole 1106 (FIG. 6) provided in proximal end 1103 of elongate channel 1102. Attached to the proximal end 1103 of the elongate channel 1102 by a spring pin connector 1235 (FIG. 6).

  Referring to FIGS. 64 and 65, in one embodiment, the articulation locking mechanism 1910 defines a central pinhole 1924 and includes a central spring body portion including lower release ring segments 1930 and 1932 and upper release ring segments 1940 and 1942. A lock spring assembly 1920, including 1922. Lock spring assembly 1920 is sized to be rotatably received within spine mounting hole 1254 of mounting base 1252. In one embodiment, upper release stop 1256 and lower release stop 1258 each project inwardly into spine mounting hole 1254. The joint locking mechanism 1910 further includes a release pin assembly 1950 that includes an upper release arm 1952 and a lower release arm 1954. Release pin assembly 1950 is attached to distal articulation link 1960 which is pinned to the distal end of distal articulation link 1710 'by link pin 1962. Distal articulation link 1710 'may be connected to a joint as described herein to axially move distal articulation link 1710' in a distal and proximal direction depending on the direction of desired articulation. Can interface with exercise systems. The bottom (not shown) of the release pin assembly 1950 is configured to be pivotally and slidably supported in a lower arcuate release pin slot 1260 formed in the end effector mounting assembly 1250. A second upper release arm slot 1270 is also formed in the end effector mounting assembly and is configured to movably receive the upper and lower release arms 1952 and 1954. As seen in FIG. 67, the upper balance formation 1272 protrudes into the second upper release arm slot 1270 and is configured to operably interface with the upper release arm 1952. Similarly, lower balance forming portion 1274 projects into second upper release arm slot 1270 and is configured to operably interface with lower release arm 1954.

  In the illustrated example, articulation pin 1542 is rotatably received within central pinhole 1924 of lock spring assembly 1920. The lock spring assembly 1920 includes an upper release stop 1256 received within an upper lock space 1941 formed between the upper release ring segments 1940 and 1942, and a lower release stop 1258 between the lower release ring segments 1930 and 1932. It is received in the spine mounting hole 1254 of the end effector mounting assembly 1250 so as to be located in the lower locking space 1931 formed therebetween. FIG. 67 shows the surgical end effector 1100 in a non-articulated position. As seen in FIG. 67, the upper release stop 1256 is in abutting engagement with the upper release ring segment 1940. Lower release stop 1258 can also abut and engage lower release ring segment 1932. Such an arrangement retains lock spring assembly 1920 in frictional engagement with articulation pin 1542 to hold surgical end effector 1100 in a non-articulated position.

  FIG. 68 is a top view of the joint lock mechanism 1910 when the surgical end effector starts joint movement to the right (arrow RD) about the joint movement axis. As seen in FIG. 68, the right articulation process is initiated by axially advancing the distal articulation link 1710 'in the distal direction DD. Advancement of the distal articulation link 1710 'in the distal direction causes the distal articulation link 1960 to move the release pin assembly 1950 in the distal direction, thereby causing the upper release arm 1952 to move the end effector mounting assembly 1250 The upper balance forming portion 1272 is brought into abutment engagement with the upper balance forming portion 1272. Such contact between the upper balance formation 1272 and the upper release arm 1952 causes the upper release arm 1952 to contact the upper release ring segment 1942 and apply a right articulation force RAF. Such movement causes the upper release ring segment 1942 to move in a counterclockwise CCW, thereby causing the lock spring assembly 1920 to open or expand and disengage from frictional engagement with the articulation pin 1542. FIG. 69 is a bottom view of the joint lock mechanism 1910 shown in FIG. As seen in FIG. 69, lower release stop 1258 abuts lower release ring segment 1930, thereby preventing lower release ring segment 1930 from moving. As a result, the lock spring assembly 1920 expands to release the articulation pin 1542. As the distal articulation link 1710 'is advanced further distally, the release pin assembly 1950 applies articulation to the surgical end effector mounting assembly 1250 in the right direction RD while simultaneously moving the lock spring assembly 1920. Release from lock engagement with articulation pin 1542. See FIG. 70. When the distal articulation link 1710 'is moved proximally to cause the surgical end effector 1100 to articulate to the left, the release pin assembly causes the lock spring assembly 1920 to expand, causing the surgical end The effector mounting assembly 1250 is moved in the opposite but similar manner to the left. Thus, as can be appreciated from the foregoing description, the lock spring assembly includes a first locked or retaining configuration in which the lock spring assembly 1920 frictionally engages the articulation pin 1542, and an additional articulation. Once locked, lock spring assembly 1920 essentially comprises a spring assembly that is expandable from a second unlocked position that freely pivots about articulation pin 1542 with surgical end effector mounting assembly 1250.

  FIGS. 71-77 illustrate an alternative joint locking mechanism 2010 for locking the surgical end effector 1100 in a position articulated about a shaft axis SA about the articulation axis BB. In the illustrated example, the surgical end effector 1100 is pivotally connected to a spine assembly 1500 '. Spine assembly 1500 'may be attached to chassis 1800 (FIG. 4) in the manner described above. The distal end portion 1540 of spine assembly 1500 'is formed with a downwardly projecting articulation pin 1542 defining an articulation axis BB. Articulating pin 1542 is configured to be rotatably or pivotally received within a spine mounting hole 1254 provided in mounting base 1252 'of end effector mounting assembly 1250'. End effector mounting assembly 1250 ′ extends through lateral mounting hole 1251 of mounting assembly 1250 ′ and is received in a channel mounting hole 1106 (FIG. 6) provided in proximal end 1103 of elongated channel 1102. Attached to the proximal end 1103 of the elongate channel 1102 by a spring pin connector 1235 (FIG. 6) provided.

  With reference to FIGS. 71 and 73, in one embodiment, the articulation locking mechanism 2010 includes a ball retainer base 2022 having a central pivot hole 2024 configured to receive an articulation pin 1542 therethrough. , A ball lock assembly 2020. The ball retainer base 2022 is attached to the articulation lock link 1960 by an articulation pin 2023 and the articulation pin 2023 passes through the pin hole 2025 of the ball retainer base 2022 and the mounting base 1252 'of the surgical end effector mounting assembly 1250'. Extend into the articulation slot 1264. The articulation link 1960 is pinned to the distal end of the distal articulation link 1710 'by a link pin 1962. Distal articulation link 1710 'may be connected to a joint as described herein to axially move distal articulation link 1710' in a distal and proximal direction depending on the direction of desired articulation. Can interface with exercise systems. Ball retainer base 2022 includes a distal locking surface 1263 formed on lock cradle 1262 on surgical end effector mounting assembly 1250 ′ and a proximal locking surface formed on distal end portion 1540 of spine assembly 1500 ′. It further includes two upright ball stoppers 2026 and 2028 which serve to hold the two lock balls 2030 and 2032 between them. The ball retainer base 2022 further includes two centering springs 2034 and 2036 that also function to support the lock balls 2030, 2032, respectively.

  FIG. 73 shows the surgical end effector 1100 in a non-articulated position. As seen in FIG. 73, a locking ball 2030, 2032 locks between the distal locking surface 1263 on the locking cradle 1262 and the proximal locking surface 1541 on the distal end portion 1540 of the spine assembly 1500 '. Captured in a mating condition, holding the surgical end effector 1100 in a non-articulated position. FIG. 74 shows the locking plane LP extending through the point of contact between the locking ball 2030 and the distal and proximal locking surfaces 1263 and 1541 on the lock cradle 1262. FIG. 75 is a top view of the joint lock mechanism 2010 when the surgical end effector starts joint movement to the right (arrow RD) about the joint movement axis. As seen in FIG. 75, the right articulation process is initiated by axially advancing the distal articulation link 1710 'in the distal direction DD. Advancement of distal articulation link 1710 'in the distal direction causes articulation link 1960 to move articulation pin 2023 distally in articulation slot 1264 in mounting base 1252' of end effector mounting assembly 1250 '. Move, and at the same time, release load RL is applied to ball retainer base 2022. Movement of the ball retainer base 2022 in the right direction RD causes the ball stopper 2026 to move the lock ball 2032 and out of lock engagement with the distal lock surface 1263 on the lock cradle 1262. Ball stop 2026 initially moves out of engagement with lock ball 2030, but lock ball 2030 temporarily engages distal lock surface 1263 and proximal lock surface 1541 on lock cradle 1262. It remains. As the distal articulation link 1710 'is advanced further distally, the articulation pin 2023 applies articulation to the surgical end effector mounting assembly 1250' in the right direction RD while simultaneously moving the ball retainer base 2022 in the right direction. Move to RD. The joint angle AA represents the amount of joint movement experienced by the surgical end effector 1100. As the ball retainer base 2022 moves rightward RD, the lock ball 2030 also moves out of lock engagement with the distal lock surface 1263 and the proximal lock surface 1541. Ball stop 2028 also holds lock ball 2032 out of lock engagement with distal locking surface 1263 and proximal locking surface 1541 during articulation. Once the surgical end effector 1100 is articulated to the desired position, distal advancement of the distal articulation link 1710 'is discontinued. Thereafter, centering springs 2034 and 2036 urge locking balls 2030 and 2032 into locking engagement with distal locking surface 1263 and proximal locking surface 1541 to hold surgical end effector 1100 in an articulated position. As seen in FIG. 76, when in the locked articulated position, the centering spring biases the locking balls 2030, 2032 to resiliently engage the distal locking surface 1263 and the proximal locking surface 1541. The effect further causes movement of the articulation pin 2023 to a neutral position within the articulation slot 1264. When the distal articulation link 1710 'is moved in a proximal direction to articulate the surgical end effector 1100 to the left, this causes the ball lock assembly 2020 and the surgical end effector 1100 to pivot to the left. Work in a similar manner.

  FIGS. 78-82 show an alternative joint locking mechanism 2110 for locking the surgical end effector 1100 in a position articulated about the shaft axis SA about the articulation axis BB. In the illustrated example, the surgical end effector 1100 is pivotally connected to a spine assembly 1500 ''. Spine assembly 1500 '' may be attached to chassis 1800 (FIG. 4) in the manner described above. The distal end portion 1540 'of the spine assembly 1500 "includes a pivot hole 1543 that defines an articulation axis BB. End effector mounting assembly 1250 ″ extends through a lateral mounting hole 1251 of mounting assembly 1250 ″ and within a channel mounting hole 1106 (FIG. 6) provided within proximal end 1103 of elongated channel 1102. Attached to the proximal end 1103 of the elongate channel 1102 by a spring pin connector 1235 (FIGS. 80-82) received at In the illustrated embodiment, the surgical end effector mounting assembly 1250 '' extends upwardly from the mounting base 1252 to form a tapered mounting column 1253 received in a pivot hole 1543 of the spine assembly 1500 ''. Including. In one mechanism, the tapered mounting column 1253 tapers away from the mounting base 1252. In other words, the cross-sectional area of the end 1255 of the tapered mounting column 1253 is smaller than the cross-sectional area of a portion of the tapered mounting column 1253 adjacent to the mounting base 1252.

  The joint lock mechanism 2110 includes at least one lock member or lock shoe movably supported between the mounting column 1253 and the inner wall 1545 of the pivot hole 1543. In the illustrated mechanism, the mounting column 1253 has a triangular cross-sectional shape that defines three column sides 1280, 1282, 1284. Thus, (in the example shown) three lock members or lock shoes 2112, 2114, 2116 are used, the lock shoe 2112 is located adjacent to the column wall 1282, and the lock shoe 2114 is adjacent to the column wall 1284. The lock shoe 2116 is arranged adjacent to the column wall 1280. A mounting column having other shapes and other numbers of lock shoes can also be used. The lock shoes 2112, 2114, 2116 are each received on a corrugated washer 2120 mounted on a mounting base 1252 of the end effector mounting assembly 1250 ''. The illustrated mechanism includes a proximal closure member 2410 that can be axially advanced and retracted in various ways as described herein, for example, with respect to the proximal closure member 1410. Proximal closure member 2410 is pivotally coupled to distal closure member 2430 that is similar in construction and operation to distal closure member 1430. As seen in FIGS. 80-82, distal closure member 2430 is connected to proximal closure member 2410 by upper dual pivot link 1220 and lower dual pivot link 1222 '. In one embodiment, the lower double pivot link 1222 'is formed with a tapered ramp 1226 on its upper surface 1224. See FIG. 78. The illustrated mechanism uses two articulation links 1710R and 1710L to apply left and right articulation to the surgical end effector 1100. See FIG. 79. To articulate the surgical end effector 1100 to the right, the articulation link 1710R is retracted axially in the proximal direction PD and the articulation link 1710L is advanced axially in the distal direction DD. Conversely, articulation link 1710L is axially retracted proximally PD and articulation link 1710R is axially advanced distally DD to articulate surgical end effector 1100 to the left. . An articulation control motion may be generated and applied to the articulation links 1710R, 1710L by various known articulation system mechanisms and other articulation system mechanisms disclosed herein. Articulation link 1710R has a slotted end portion 1711R that is received on a right articulation pin 1266R mounted on end effector mounting assembly 1250 ''. Similarly, articulation link 1710L has a slotted end portion 1711L that is received on a left articulation pin 1266L attached to end effector mounting assembly 1250 ''.

  Referring now to FIG. 80, in the illustrated mechanism, the corrugated washer 2120 biases the mounting base 1252 of the end effector mounting assembly 1250 ″ downward (arrow D) when the closure system is inactive. . In FIG. 80, the proximal closure member 2410 is in a proximal position. Similarly, the lower double pivot link 1222 'is also in a proximal position that allows the mounting base 1252 to be driven downward. Because the mounting base 1252 is in the lowest or unlocked position, the tapered mounting column 1253 causes the locking shoes 2112, 2114, 2116 is released (first unlocked position). Thus, when in that position, the surgical end effector 1100 can be articulated about the articulation axis BB by the articulation links 1710R, 1710L. Once the surgical end effector 1100 is articulated to a desired position, the articulation locking mechanism 2110 can be reactivated by advancing the proximal closure member 2410 distally.

  FIG. 81 shows the start of the lock process. As can be seen in this figure, the proximal closure member 2410 and the lower double pivot link 1222 'are first moved in the distal direction DD. As the lower dual pivot link 1222 'moves distally, the ramp 1226 thereon drives the mounting base 1252 of the end effector mounting assembly 1250 "upward to collapse the corrugated washer 2120. As the mounting base 1252 moves upward (arrow U), the tapered mounting column 1253 causes the locking shoes 2112, 2114, 2116 to move from the first unlocked position to the distal end portion 1540 'of the spine assembly 1500' '. ′ To resiliently engage the second lock position (second locked position) to lock the surgical end effector 1100 in the articulated position. This locking of the surgical end effector 1100 occurs before the jaws of the surgical end effector are completely closed. FIG. 82 illustrates the position of the proximal closure member 2410, lower double pivot link 1222 ′, and articulation locking mechanism 2110 when the closure system component is moved to a fully closed position where the end effector is completely closed. Show. Thus, the joint locking mechanism 2110 can be activated or moved between a locked state and an unlocked state by actuating the closure system by a small amount. An alternative mechanism is envisioned in which the mounting column is attached to the distal end of the spine assembly and a pivot hole is provided in the proximal portion of the surgical end effector.

  FIGS. 83 and 84 show an alternative articulation locking mechanism 2110 'for locking the surgical end effector 1100 in a position articulated about a shaft axis SA about the articulation axis BB. In the illustrated example, the surgical end effector 1100 is pivotally connected to a spine assembly 1500 ''. Spine assembly 1500 '' may be attached to chassis 1800 (FIG. 4) in the manner described above. The distal end portion 1540 'of the spine assembly 1500 "includes a pivot hole 1543 that defines an articulation axis BB. End effector mounting assembly 1250 ″ extends through lateral mounting hole 1251 of mounting assembly 1250 ″ and into a channel mounting hole 1106 (FIG. 6) provided in proximal end 1103 of elongated channel 1102. Attached to the proximal end 1103 of the elongate channel 1102 by a received spring pin connector 1235 (FIG. 6). The surgical end effector mounting assembly 1250 "includes a mounting column 1253" extending upwardly from the mounting base 1252 and received in a pivot hole 1543 of the spine assembly 1500 ". In this embodiment, the mounting column 1253 'need not be tapered.

  This embodiment also includes a plurality of lock shoes 2112 ', 2114', 2116 ', each manufactured from an electro-activated polymer material (EAP). Such a material may expand, for example, when electrically excited. For example, current may be applied to one or more of the lock shoes 2112 ', 2114', 2116 'by conductors (not shown) extending from the housing or handle mechanism or robot control system or the like. Thus, once the surgical end effector 1100 is articulated to a desired position, one or more of the lock shoes 2112 ', 2114', 2116 'are expanded by applying a current thereto. You. In other mechanisms, one or more of the lock shoes 2112 ', 2114', 2116 'may be configured to be pneumatically or hydraulically inflated. In other arrangements, the lock shoes 2112 ', 2114', 2116 'may not be expandable. In such a mechanism, the mounting column 1253 may be made from EAP and selectively expandable by applying a current thereto. In other arrangements, the mounting column 1253 may be selectively expandable pneumatically or hydraulically.

  FIGS. 85-89 show an alternative articulation locking mechanism 2210 for locking the surgical end effector 1100 in a position articulated about a shaft axis SA about the articulation axis BB. In the illustrated example, the surgical end effector 1100 is pivotally connected to a spine assembly 1500 '. Spine assembly 1500 'may be attached to chassis 1800 (FIG. 4) in the manner described above. The distal end portion 1540 of the upper portion 1539 of the spine assembly 1500 'is formed with a downwardly projecting articulation pin 1542 defining an articulation axis BB. Articulating pin 1542 is configured to be rotatably or pivotally received within a spine mounting hole 1254 provided in mounting base 1252 of end effector mounting assembly 1250 ''. End effector mounting assembly 1250 ″ extends through lateral mounting hole 1251 of mounting assembly 1250 ″ and into a channel mounting hole 1106 (FIG. 6) provided at proximal end 1103 of elongated channel 1102. Attached to the proximal end 1103 of the elongate channel 1102 by a received spring pin connector 1235 (FIG. 6).

  Referring to FIG. 85, the illustrated mechanism uses two articulation links 1710R 'and 1710L' to apply left and right articulation to the surgical end effector 1100. However, in other embodiments, only one articulation link may be used. In the illustrated mechanism, the articulation link 1710R 'is retracted axially in the proximal direction PD and the articulation link 1710L' is axially retracted in the distal direction DD to articulate the surgical end effector 1100 to the right. Will be advanced. Conversely, articulation link 1710L 'is axially retracted proximally PD and articulation link 1710R' is axially advanced distally DD to articulate surgical end effector 1100 to the left. Is done. Articulation link 1710R 'has a slotted end portion 1711R that is received on a right articulation pin 1266R attached to end effector mounting assembly 1250 ". Similarly, articulation link 1710L 'has a slotted end portion 1711L that is received on a left articulation pin 1266L attached to end effector mounting assembly 1250 ".

  With further reference to FIG. 85, the articulating locking mechanism 2210 in the illustrated embodiment includes a locking assembly 2220 including a distal end 2222 having a right locking member or fork 2224 and a left locking member or fork 2228 projecting therefrom. The right locking member 2224 includes a right locking gear rack 2226 laterally adjacent and facing the corresponding right articulating gear rack 1720 formed on a portion extending below the right articulating link 1710R '. Similarly, left locking member 2228 is laterally adjacent to and faces a corresponding left articulating gear rack 1723 formed on portion 1722 extending below left articulating link 1710L '. 2230. In the inoperative state, the right locking member 2224 and the left locking member 2228 are located at the center between the right articulation link 1710R 'and the left articulation link 1710L', and are not engaged with them. As further seen in FIG. 85, locking assembly 2220 is supported between lower distal spine portion 1550 and upper spine portion 1539. The lower distal spine portion 1550 extends through a mounting hole 2223 in the distal end 2222 of the locking assembly 2220 and is received in a distal boss 1544 formed below the upper spine portion 1539 and upwardly. An extending distal support pin 1554 is included. See FIG. 86. Lower distal spine portion 1550 extends between right locking member 2224 and left locking member 2228 through locking opening 2225 and into a proximal boss 1546 formed below upper spine portion 1539. It further includes an upwardly extending proximal support pin 1556 that is received.

  In the mechanism shown, the articulation locking mechanism 2210 also includes an axially movable lock bar assembly 2240 that operably interfaces with an articulation transmitter 2250 operably supported within the shaft assembly 1400 '. Lock bar assembly 2240 includes a lock wedge 2244 formed on a distal end 2242 thereof. Articulation transmitter 2250 is configured to operably interface with distal firing bar 1620 operably supported within shaft assembly 1400 '. In this context, distal firing bar 1620 may include a firing actuator.

  Referring now to FIGS. 85-87, in the mechanism shown, one form of articulation transmitter 2250 is formed on a portion of distal firing bar 1620 and a shifter drive rack 2254 formed on shifter 2252. Include a firing rack 1624 configured to operably engage. The proximal end 2253 of the shifter 2252 is configured to operably interface with a lock bar coupler 2246 formed on the lock bar assembly 2240. As further seen in FIGS. 85-87, shifter 2252 further includes a shifter driven rack 2256 that meshes with an articulating pinion gear 2262 mounted on articulating sprocket gear 2260. Articulating sprocket gear 2260 is rotatably supported within shaft assembly 1400 'and is in mating engagement with a right mating engagement drive rack 1724 formed on or attached to right distal articulation link 1710R'. Not only is it in mating engagement with a left articulation drive rack 1726 formed on or otherwise attached to the left distal articulation link 1710L '.

  The operation of the joint motion transmitter 2250 and the joint lock mechanism 2210 will be described with reference to FIGS. FIG. 87 shows the surgical end effector 1100 in a non-articulated position. The lock bar assembly 2240 is in its most distal “unlocked position” and the lock wedge 2244 is received in a lock opening 2225 located between the right lock member 2224 and the left lock member 2228. . The right and left locking members 2224, 2228 are in their inactive state and are not engaged with the right and left articulation links 1710R ', 1710L'. Thus, the right lock gear rack 2226 on the right lock member 2224 is out of engagement with the right articulation gear rack 1720 on the right distal articulation link 1710R ', and the left lock gear rack 2230 is disengaged from the left distal articulation link. 1710L 'is out of meshing engagement with left articulating gear rack 1723. Accordingly, the joint lock mechanism 2210 is in an "unlocked" configuration. However, friction between the various components may prevent the surgical end effector 1100 from flopping or rotating about the articulation axis BB.

  FIG. 88 shows the start of the articulation process. As seen in FIG. 88, the proximal end 2253 of the shifter 2252 is operably engaged with the lock bar coupler 2246 and the lock bar assembly 2240 is in the unlocked orientation. When shifter 2252 is thus engaged with lock bar assembly 2240, shifter drive rack 2254 is in mating engagement with firing rack 1624 on distal firing bar 1620. Subsequently, the articulation process is initiated by moving distal firing bar 1620 in an axial direction. In the example shown in FIG. 88, the end effector 1100 is articulated to the right RD about the articulation axis by axially moving the distal firing bar 1620 in the proximal direction PD. Axial actuation of the distal firing bar 1620 in the proximal and distal directions has been discussed in detail herein. Lock bar coupler 2246 holds shifter drive rack 2254 in mating engagement with firing rack 1624 on distal firing bar 1620 so that shifter 2252 moves proximally with distal firing bar 1620. . Movement of the shifter 2252 in the proximal direction PD by the meshing engagement of the shifter driven rack 2256 and the articulation pinion gear 2262 causes the articulation pinion gear 2262 and the articulation sprocket gear 2260 to rotate clockwise via the articulation operating angle AAA. Rotate in the direction. As the articulation sprocket gear 2260 rotates, the right distal articulation link 1710R 'is driven in the proximal direction PD and the left distal articulation link 1710L' is driven in the distal direction DD, which ultimately drives the surgical The end effector pivots rightward RD about the articulation axis. Once the surgical end effector 1100 is articulated to the desired position, the user advances the lock bar assembly 2240 axially in the proximal direction PD, thereby moving the lock wedge 2244 proximally to the right. Driving contact is made with two actuating detents 2227, 2229 formed on the locking member 2224 and the left locking member 2228, respectively, so that the right locking member 2224 and the left locking member 2228 are laterally outwardly and laterally. The end effector 1100 can be locked in its articulated position by biasing and lockingly engaging the right and left articulating gear racks 1720, 1723, respectively. Such proximal movement of lock bar assembly 2240 further serves to separate lock bar coupler 2246 from shifter 2252, as shown in FIG.

  As seen in FIG. 89, when the shifter 2252 is separated from the lock bar assembly 2240, the shifter drive rack 2254 is no longer in meshing engagement with the firing rack 1624 on the distal firing bar 1620 and the shifter driven rack 2256 Is no longer in meshing engagement with the articulating pinion gear 2262. Thus, at this point, the distal firing bar 1620 can be advanced distally to apply firing motion to the surgical end effector, and then proximally retracted to the starting position shown in FIG. Once the distal firing bar 1620 returns to the starting position, the user can then advance the lock bar assembly 2240 distally to operably engage the lock bar coupler 2246 with the proximal end 2253 of the shifter 2252. Lock wedge 2244 can be returned to its starting or unlocked position, where right lock member 2224 and left lock member 2228 bounce back or otherwise to these unlocked positions. You can go back. Subsequently, the user can apply axial movement to distal firing bar 1620 in the appropriate axial direction to return surgical end effector 1100 to its non-articulated position.

  FIGS. 90-95 show an alternative joint locking mechanism 2310 for locking the surgical end effector 1100 in a position articulated about a shaft axis SA about the articulation axis BB. In the illustrated example, the surgical end effector 1100 is pivotally connected to a spine assembly 1500 '. Spine assembly 1500 'may be attached to chassis 1800 (FIG. 4) in the manner described above. The distal end portion 1540 of the upper spine portion 1539 of the spine assembly 1500 'is formed with a downwardly projecting articulation pin 1542 that defines an articulation axis BB. Articulating pin 1542 is configured to be rotatably or pivotally received within a spine mounting hole 1254 provided in mounting base 1252 of end effector mounting assembly 1250 ''. End effector mounting assembly 1250 ″ extends through a lateral mounting hole 1251 of mounting assembly 1250 ″ and within a channel mounting hole 1106 (FIG. 6) provided within proximal end 1103 of elongated channel 1102. Attached to the proximal end 1103 of the elongate channel 1102 by a spring pin connector 1235 (FIG. 6) that is received at

  Referring to FIG. 90, the illustrated mechanism uses two articulation links 1710R '' and 1710L '' to apply right and left articulation to the surgical end effector 1100. To articulate the surgical end effector 1100 to the right, the articulation link 1710R "is retracted axially in the proximal direction PD and the articulation link 1710L" is advanced axially in the distal direction DD. . Conversely, to articulate the surgical end effector 1100 to the left, the articulation link 1710L "is retracted axially in the proximal direction PD and the articulation link 1710R" is axially retracted in the distal direction DD. Is advanced to Right distal articulation link 1710R "" has a slotted end portion 1711R that is received on a right articulation pin 1266R mounted to end effector mounting assembly 1250 ". Similarly, left distal articulation link 1710L '' has a slotted end portion 1711L that is received on a left articulation pin 1266L attached to end effector mounting assembly 1250 ''.

  Referring still to FIG. 90, a right brake plate 2312 is formed on the right distal articulation link 1710R '', and a left brake plate 2320 is formed on the left distal articulation link 1710L ''. As further seen in FIG. 90, the right and left brake plates 2312, 2320 are supported between a lower distal spine portion 1552 'and an upper spine portion 1539. Lower distal spine portion 1552 ′ includes an upwardly extending distal support pin 1554 configured to be received within a distal boss (not shown) formed below upper spine portion 1539. Including. In the mechanism shown, the articulation locking mechanism 2310 also operably interfaces with an articulation transmitter of the type described herein, or otherwise, in the distal direction DD and the proximal direction PD. Includes an axially movable and lockable lock bar assembly 2340 that can interface with a lock bar control mechanism (not shown) configured to apply axial control movement. Lock bar assembly 2340 includes a lock clamp 2344 formed on its distal end 2342. Lock clamp 2344 extends through right brake slot 2314 in right brake plate 2312 and left brake slot 2322 in left brake plate 2320, as well as through axial slot 2352 provided through wedge plate 2350. And engage the clamp plate 2360.

  The operation of the joint lock mechanism 2310 will be described below with reference to FIGS. FIG. 91 shows the surgical end effector 1100 in a non-articulated position. Lock bar assembly 2340 is in the unlocked position, where clamp portion 2344 does not apply any clamping force to right and left brake plates 2312, 2320. Thus, the right distal articulation link 1710R "and the left distal articulation link 1710L" are free to move axially when articulation is applied. Due to friction between various components, the surgical end effector 1100 may not be able to flop or rotate about the articulation axis BB. FIG. 92 illustrates a surgical end effector 1100 by axially moving a right distal articulation link 1710R ″ in a distal direction DD and moving a left distal articulation link 1710L ″ in a proximal direction PD. Shows the joint movement to the left LD in FIG. FIG. 93 shows the joint locking mechanism 2310 in an unlocked configuration. FIGS. 94 and 95 show the joint locking mechanism 2310 in a locked configuration. The articulation locking mechanism 2310 is locked by applying an actuation motion proximally to the lock bar assembly 2340. With such action, its clamp portion for clamping the right and left brake plates 2312, 2320 is held clamped between the wedge plate 2350 and the lower distal spine portion 1552 '. Such a mechanism applies a clamping force CF between the clamp plate 2360 and the lower distal spine portion 1552 ', thereby causing the right distal articulation link 1710R "and the left distal articulation link 1710L" to move. Serves to prevent any further axial movement.

  FIGS. 96 and 97 illustrate one example of an articulation stroke amplifier transmission mechanism 2410 that may be used with the various articulation linkages disclosed herein. Referring first to FIG. 97, a cross-sectional view of a portion of a shaft assembly 1400 ″ including a proximal closure member 1410 and an upper intermediate spine segment 1510 ″ and a distal spine extension 1562 ″ is shown. Intermediate spine segment 1510 "and distal spine extension 1562" serve to operatively support distal firing bar 1620 and proximal firing shaft segment 1602 in various manners as disclosed herein. This embodiment includes an intermediate articulation link segment 1706 and a distal articulation link segment 1707 that can interface with the end effector mounting assembly in any of the various ways disclosed herein. The intermediate articulation link 1706 can operatively interface with the articulation lock 1210 in a variety of ways as disclosed herein. As seen in FIG. 96, the intermediate articulation link segment 1706 includes an intermediate or first gear rack 1708 formed thereon, and the distal articulation link segment 1707 includes a second or distal gear rack 1709. Including. Gear racks 1708 and 1709 are in mesh with at least one, and preferably at least two, amplifier pinion gear sets 2412 rotatably supported between upper middle spine segment 1510 "and distal spine extension 1562". I agree. See FIG. 97. In the illustrated mechanism, for example, each amplifier gear set 2412 has a smaller drive gear 2414 supported in meshing engagement with the first gear rack 1708 and a larger amplifier gear 2416 supported in meshing engagement with the distal gear rack 1709. And.

98A-98C illustrate the operation of the articulation stroke amplifier transmission mechanism 2410. FIG. 98A shows the position of the intermediate articulation link segment 1706 and the distal articulation link segment 1707 when in a neutral or non-articulated position. FIG. 98B illustrates the position of the intermediate articulating link segment 1706 and the distal articulating link segment 1707 after the intermediate articulating link segment 1706 has been axially advanced distally from the neutral position of FIG. 98A by a distance D _1R. Is shown. As further seen in FIG. 98B, the distal articulation link 1707 has moved an axial distance _D2R . In the illustrated example, D _2R > D _1R . FIG. 98C illustrates the intermediate articulating link segment 1706 and the distal articulating link segment after the intermediate articulating link segment 1706 has been axially advanced in the proximal direction PD by a distance D _1L from the neutral position shown in FIG. 98A. The position of 1707 is shown. As further seen in FIG. 98C, the distal articulation link 1707 has moved an axial distance _D2L . In the illustrated example, D _2L > D _1L . Thus, such a mechanism allows additional axial articulation strokes to be obtained and used to articulate the end effector through a larger articulation range about the articulation axis.

  FIGS. 99A and 99B illustrate an example of an articulation stroke amplifier transmitter 2510 that may be used with the various articulation linkages disclosed herein. The articulation stroke amplifier 2510 is operatively interfaced with the proximal articulation driver 1700 ″, and the proximal articulation driver 1700 ″ is identical to the proximal articulation driver 1700 except for the differences described above. They may be the same. Specifically, proximal articulation driver 1700 '' includes a drive rack 1701 formed on its distal end. The drive rack is configured to mesh with a gear segment 2522 formed on a swing gear 2520 that is pivotally pinned to a corresponding portion of the spine assembly. In the mechanism shown, the swing gear 2520 is pivotable about an axially transverse swing gear axis configured to move the proximal articulation driver 1700 ''. Swing gear 2520 further includes a transfer slot 2524 configured to receive a transfer pin 1713 attached to proximal end 1716 of intermediate articulation link segment 1706 ″. As seen in FIGS. 99A-99B, the distal end of the intermediate articulation link segment 1706 '' is configured to operably interface with the articulation lock 1210 in various ways as disclosed herein. .

FIG. 99A shows articulation stroke amplifier transmitter 2510 in a neutral position where articulation has not been applied to proximal articulation driver 1700 ″. Figure 99B shows the position of the articulation stroke amplifier transfer machine 2510 after proximal articulation driver 1700 '' have been advanced to a first axial distance D ₁ only axially in the distal direction DD. Such movement of the proximal articulation driver 1700 ″ in the distal direction causes the swing gear 2520 to pivot in a clockwise direction CW about the swing gear axis. Such movement of swing gear 2520 drives intermediate articulation link segment 1706 '' in a proximal direction by a _second axial distance D2. In such an example, D ₂ > D ₁ . 99C-99D illustrate a similar mechanism, except that a transfer slot 2524 is provided on the proximal end 1716 of the intermediate articulation link segment 1706 '' and a transfer pin 1713 is provided on the swing gear 2520.

  Example 1-A surgical tool assembly comprising a surgical end effector movably connected to a shaft assembly by an articulation. The articulation is configured to selectively promote selective articulation of the surgical end effector relative to the shaft assembly about the articulation axis. The articulation axis traverses the shaft axis defined by the shaft assembly. The shaft assembly includes a proximal end, a distal end operably connected to the articulation, and an elongated notch in the shaft assembly. An elongate notch is on one side of the shaft axis and is located adjacent the distal end.

  Example 2-The surgical tool of example 1, wherein the articulation is configured to limit articulation of the surgical end effector about the articulation axis to one side of the shaft axis. assembly.

  Example 3-The surgical tool assembly of Examples 1 or 2, wherein the shaft assembly comprises a spine assembly and a proximal closure member. The spine assembly includes a distal spine end operatively connected to an articulation. A proximal closure member is supported on the spine assembly for selective axial movement with respect to the spine assembly. The elongated notch has an elongated spine notch in the distal spine end on one side of the shaft axis and an elongated closure notch in the proximal closure member on one side of the shaft axis and corresponding to the elongated spine notch. And further comprising:

  Example 4-Surgical end effector includes a first jaw operatively connected to an articulation and a selectively movable movement relative to the first jaw in response to an applied closing motion. A surgical tool assembly according to example 3, comprising a second jaw supported.

  Example 5 The shaft assembly further comprises a distal closure member movably connected to the proximal closure member for selective axial movement with the proximal closure member, the distal closure member comprising a second closure member. The surgical tool assembly of claim 4, wherein the surgical tool assembly is operably interfaced with the jaw to apply a closing motion to the second jaw.

  Example 6-The surgical tool assembly of Example 1 or further comprising means for preventing buckling of the distal end of the shaft assembly when axial actuation motion is applied to the proximal end of the shaft assembly. 3. The surgical tool assembly of claim 2.

  Example 7-The surgical tool assembly according to Example 3, wherein the surgical tool assembly further comprises means for preventing buckling of the distal end of the shaft assembly when an axial actuation motion is applied to the proximal end of the shaft assembly. A surgical tool assembly according to claim 4 or 5.

  Example 8-Example 7 wherein the means for preventing buckling comprises at least one alignment member projecting from the proximal closure member and extending into a corresponding axial slot in the spine assembly. Surgical tool assembly.

  Example 9-At least one alignment member projects from a proximal closure member at a first position and extends into a corresponding first axial slot in a spine assembly for axial movement therein. An at least one first alignment member, and at least one second alignment member projecting from the proximal closure member at a second position diametrically opposite the first position. The surgical tool assembly according to Example 8. A second alignment member extends into a corresponding second axial slot in the spine assembly.

  Example 10-The surgical tool assembly of Examples 8 or 9, wherein at least one of the at least one alignment member has an L-shaped cross-sectional shape.

  Example 11-A surgical tool assembly, comprising a surgical end effector movably connected to a shaft assembly by an articulation joint. The articulation is configured to facilitate selective articulation of the surgical end effector relative to the shaft assembly about the articulation axis. The articulation axis traverses the shaft axis defined by the shaft assembly. The shaft assembly includes a proximal portion including an uninterrupted outer proximal perimeter, and a distal portion extending from the proximal portion and operatively connected to an articulation joint. . The distal portion includes a distal periphery including a discontinuous distal portion located on one side of the shaft axis.

  Example 12-The surgical tool of example 11, wherein the articulation is configured to limit articulation of the surgical end effector about the articulation axis to one side of the shaft axis. assembly.

  Example 13-A shaft assembly is supported on a spine assembly for selective axial movement relative to the spine assembly and a spine assembly having a distal spine end operably coupled to an articulation joint. 13. The surgical tool assembly according to example 11 or 12, comprising a proximal closure member. The discontinuous distal portion includes an elongated closure notch in the proximal closure on one side of the shaft axis.

  Example 14-The surgical tool assembly of Example 13, wherein the surgical tool assembly further comprises an elongated closure member notch.

  Example 15-The surgical tool assembly of Example 13 or further comprising means for preventing buckling of the distal end of the shaft assembly when axial actuation motion is applied to the proximal portion of the shaft assembly. 15. The surgical tool assembly according to claim 14.

  Example 16-Example 15 wherein the means for preventing buckling comprises at least one alignment member projecting from the proximal closure member and extending into a corresponding axial slot in the spine assembly. Surgical tool assembly.

  Example 17-at least one alignment member projects from a proximal closure member at a first position, extends into a corresponding first axial slot in a spine assembly, and moves axially therein. An embodiment comprising at least one first alignment member and at least one second alignment member protruding from a proximal closure member at a second position diametrically opposite the first position. 17. The surgical tool assembly according to claim 16. A second alignment member extends into a corresponding second axial slot in the spine assembly.

  Example 18-The surgical tool assembly of Examples 16 or 17, wherein at least one of the at least one alignment member has an L-shaped cross-sectional shape.

  Example 19-The surgical tool assembly of Examples 11, 12, 13, 14, 15, 16, 17, or 18 wherein the distal portion includes a distal axial length. The proximal portion includes a proximal axial length, wherein the proximal axial length is longer than the distal axial length.

  Example 20-A surgical tool assembly, comprising a surgical end effector movably connected to a shaft assembly by an articulation joint. The articulation is configured to facilitate selective articulation of the surgical end effector relative to the shaft assembly about the articulation axis. The articulation axis traverses the shaft axis defined by the shaft assembly. The shaft assembly includes a proximal end, a distal end operatively connected to the articulation joint, an elongated notch, and an axially displaceable firing member axially aligned with the shaft axis. The elongate notch is within the shaft assembly on one side of the shaft axis and is located adjacent the distal end.

  Example 21-A surgical tool assembly, comprising a shaft assembly, a surgical end effector, and a protective cap member. The shaft assembly includes an axially movable closure member and an axially movable firing member selectively axially movable between an unfired position and a fired position. The surgical end effector includes a first jaw and a second jaw having a mounting portion including a pair of mounting walls. The mounting wall is movably engaged with a portion of the first jaw and configured to movably support the second jaw on the first jaw. The mounting portion defines a cam area configured to be engaged by an axially movable closure member to move the second jaw relative to the first jaw from an open position to a closed position. The mounting wall defines an upper open parking area between the mounting walls for accommodating the firing member when the firing member is in the unfired position. The protective cap member is attached to the mounting wall and covers at least a portion of the upper open parking area.

  Example 22-Each of the mounting walls is pivotable to a corresponding portion of the first jaw to facilitate pivotal movement of the second jaw relative to the first jaw about the pivot axis. 22. The surgical tool assembly according to example 21, wherein the surgical tool assembly is configured to engage a.

  Example 23-The surgical tool assembly of Example 22, wherein each of the mounting walls protrudes proximally from the cam area. The protective cap covers at least a portion of the upper open parking area proximal to the cam area and forms a transition portion configured to form a pre-closure cam surface proximal to the cam area, and extends from the transition section. And at least one attachment portion connecting the protective cap to at least one of the mounting walls.

  Example 24-at least one attachment member extends downwardly from the transition portion and is configured to retainably engage a corresponding one of the mounting walls; A second leg extending downwardly from the portion and configured to retainably engage a corresponding one of the mounting walls. assembly.

  Example 25-The surgical tool assembly of Example 24, wherein the first and second legs are removably attachable to the mounting wall.

  Example 26-A first mounting opening configured to retain and receive therein a first mounting lug formed on a corresponding one of the mounting walls. 26. The surgical tool assembly according to example 25, comprising: The second leg includes a second mounting opening configured to resiliently receive a second mounting lug formed on a corresponding one of the mounting walls.

  Example 27-A closure member is configured to come into engagement with a pre-closure cam surface on a protective cap and a cam area on a mounting portion to move a second jaw from an open position to a closed position. 27. The surgical tool assembly according to example 23, 24, 25 or 26, comprising a distal camming surface.

  Example 28-The surgical tool assembly of Examples 22, 23, 24, 25, 26, or 27, further comprising means for biasing the second jaw to the open position.

  Example 29-The surgical tool assembly of Example 28, wherein the surgical tool assembly further comprises means for preventing the second jaw from opening beyond a maximum open position.

  Example 30-The second jaw is configured to be selectively pivotable about a pivot axis with respect to the first jaw, wherein at least a portion of the upper open parking area is near the pivot axis. 30. The surgical tool assembly according to any of embodiments 22, 23, 24, 25, 26, 27, 28, or 29, wherein

  Example 31-The method of any of Examples 22, 23, 24, 25, 26, 27, 28, 29, or 30, wherein the second jaw comprises a pair of trunnions pivotally supported within the mounting wall. Surgical tool assembly.

  Example 32-A pair of trunnions includes a first trunnion configured to be pivotally supported within a first lateral pivot hole in a first one of the mounting walls, and a mounting wall. A second trunnion configured to be pivotally supported within a second lateral pivot hole in a second of the portions. . The first and second trunnions define a pivot axis about which the second jaw is pivotable.

  Example 33-The surgical tool assembly further comprises a first installation slot in a first one of the mounting walls and a second installation slot in a second one of the mounting walls. The surgical tool assembly according to embodiment 32. The first installation slot extends laterally from the first top edge of the first of the mounting walls to the first lateral pivot hole relative to the first lateral pivot hole. I do. A second mounting slot is formed with respect to the second lateral pivot hole from the second top edge of the second one of the mounting walls to the second lateral pivot hole. Extend laterally to

  Example 34-A surgical tool assembly, comprising a shaft assembly, a surgical end effector, and a protective cap member. The shaft assembly includes an axially movable closure member and an axially movable firing member selectively axially movable between an unfired position and a fired position. The surgical end effector includes an elongated channel configured to operatively support a surgical staple cartridge therein, and an anvil with an anvil mounting portion. The anvil mounting portion includes a pair of anvil mounting walls pivotally supported on the elongate channel for selectively pivoting relative to the elongate channel about a pivot axis. The anvil mounting portion defines a cam area configured to be engaged by an axially movable closure member to move the anvil relative to the elongate channel from an open position to a closed position. The anvil mounting wall defines an upper open parking area between the anvil mounting walls to accommodate the firing member when the firing member is in the unfired position. The protective cap member is attached to the anvil mounting wall and covers at least a portion of the upper open parking area.

  Example 35-The surgical tool assembly of Example 34, wherein at least a portion of the upper open parking area is proximal to the pivot axis.

  Example 36-The surgical device of examples 34 or 35, wherein the firing member comprises a vertically extending firing body with a tissue cutting edge, a top anvil engagement tab, and a bottom channel engagement tab. Tool assembly. The upper anvil engaging tab extends laterally from the upper end of the firing body and is configured to engage the anvil when the firing member is advanced axially from the unfired position to the fired position. A bottom channel engaging tab extends laterally from the bottom of the firing body and engages the channel to be supported within the elongated channel when the firing member is advanced axially from an unfired position to a fired position. Configured to hold the underside of the anvil a desired distance from the cartridge deck of the surgical staple cartridge.

  Example 37-The surgical tool assembly of Examples 34, 35, or 36, wherein each of the mounting walls protrudes proximally from the cam area. The protective cap covers at least a portion of the upper open parking area proximal to the cam area and forms a transition portion configured to form a pre-closure cam surface proximal to the cam area, and extends from the transition section. And at least one attachment portion connecting the protective cap to at least one of the anvil mounting walls.

  Example 38-at least one attachment portion extends downwardly from the transition portion and is configured to retainably engage a corresponding one of the anvil mounting walls; A second leg extending downwardly from the transition portion and configured to retainably engage a corresponding one of the anvil mounting walls. Tool assembly.

  Embodiment 39-The surgical tool of any of embodiments 34, 35, 36, 37, or 38, wherein the surgical tool assembly further comprises means for biasing the anvil to the open position when the closure member is in the starting position. Tool assembly.

  Example 40-A surgical tool assembly, comprising a shaft assembly and a surgical end effector. The shaft assembly includes an axially movable closure member and an axially movable firing member selectively axially movable between an unfired position and a fired position. The surgical end effector includes a first jaw and a second jaw having a mounting portion. The mounting portion includes a pair of mounting walls configured to movably engage a portion of the first jaw and to movably support the second jaw on the first jaw. The mounting portion defines a cam area configured to be engaged by an axially movable closure member to move the second jaw relative to the first jaw from an open position to a closed position. The mounting wall defines an upper open parking area between the mounting walls for accommodating the firing member when the firing member is in the unfired position. The surgical tool assembly further comprises means for at least partially covering at least a portion of the upper open parking area and defining a pre-closure cam surface proximal to the cam area.

  Example 41-A surgical tool assembly, comprising: a first jaw, a second jaw, and a shaft assembly. A second jaw is movably supported on the first jaw to selectively move between an open position and a closed position relative to the first jaw about a fixed pivot axis. I have. The shaft assembly includes an initial closing motion in a first closing direction perpendicular to the cam surface relative to the cam surface when the closing member is axially advanced over the cam surface on the second jaw; And an additional closing movement in a second closing direction that is parallel to the shaft axis.

  Example 42-A cam surface is formed on a second jaw mounting portion, wherein the second jaws are each pivotally connected to the first jaws for selectively pivoting about a pivot axis. 42. The surgical tool assembly according to embodiment 41, further comprising first and second mounting walls attached.

  Example 43-A distal closure tube including an axially movable closure member including a distal end surface and a distal camming surface configured to engage a camming surface on a second jaw. 43. The surgical tool assembly according to example 41 or 42, comprising:

  Example 44-Example 43 wherein the distal end surface is configured to apply an initial closing motion to the cam surface and the distal camming surface is configured to apply an additional closing motion to the cam surface. A surgical tool assembly as described.

  Example 45-The example of embodiment 44, wherein the distal end surface includes a portion of the cross-sectional thickness of the obturator tube, and the cumming surface extends from the distal end surface and includes another portion of the cross-sectional thickness of the obturator tube. Surgical tool assembly.

  Example 46-The surgical tool assembly of example 45, wherein the closure tube comprises an outer surface, an inner surface, and a distal end defining a distal end surface. The distal camming surface extends from the distal end surface to the inner surface at an obtuse angle to the distal end surface.

  Example 47-A shaft assembly is axially movable between a first mounting wall and a second mounting wall, selectively axially movable between a start position and an end position. 43. The surgical tool assembly according to embodiment 42, further comprising a flexible firing member.

  Example 48-The surgical tool assembly of example 47, wherein at least a portion of the firing member is proximal to the cam surface when the firing member is in the starting position.

  Example 49-A surgical tool assembly, comprising an end effector and a shaft assembly. The end effector includes an elongated channel configured to operatively support a surgical staple cartridge therein, and an anvil. The anvil includes an anvil mounting portion movably supported on the elongate channel for selectively moving between an open position and a closed position about a fixed pivot axis relative to the elongate channel. The shaft assembly defines a shaft axis, and includes an axially movable closure member, wherein the axially movable closure member is axially advanced over the cam surface on the anvil mounting portion. When performed, an initial closing movement in a first closing direction perpendicular to the cam surface relative to the cam surface and an additional closing movement in a second closing direction parallel to the shaft axis relative to the cam surface. It is configured to apply.

  Embodiment 50-The embodiment further comprises the first and second anvil mounting walls pivotally attached to the elongate channel for selective pivoting about the pivot axis. 50. The surgical tool assembly according to Example 49.

  Example 51-An axially movable closure member includes a distal closure tube including a distal end surface and a distal camming surface configured to engage a camming surface on an anvil mounting portion. 51. The surgical tool assembly according to example 49 or 50, comprising:

  Example 52-Embodiment 51 wherein the distal end surface is configured to apply an initial closing movement to the cam surface and the distal camming surface is configured to apply an additional closing movement to the cam surface. A surgical tool assembly as described.

  Example 53-The example of embodiment 52, wherein the distal end surface includes a portion of the cross-sectional thickness of the obturator tube and the cumming surface extends from the distal end surface and includes another portion of the cross-sectional thickness of the obturator tube. Surgical tool assembly.

  Example 54-A shaft assembly is selectively axially movable between a first anvil mounting wall and a second anvil mounting wall between a start position and an end position. 51. The surgical tool assembly according to embodiment 50, further comprising a movable firing member.

  Example 55-The surgical tool assembly of example 54, wherein at least a portion of the firing member is proximal of the cam surface when the firing member is in the starting position.

  Example 56-A surgical tool assembly comprising an end effector and a shaft assembly defining a shaft axis and including an axially movable closure member. The end effector includes an elongate channel configured to operatively support the surgical cartridge therein, and an end effector on the elongate channel for selectively moving between an open position and a closed position relative to the elongate channel. An anvil provided movably with an anvil mounting portion supported by the anvil. The surgical tool assembly includes a first closure means on the closure member for applying an initial closure movement in a first closure direction perpendicular to the cam surface to the cam surface on the anvil mounting portion; Second closing means for applying an additional closing movement to the cam surface in a second closing direction parallel to the shaft axis when the member is advanced axially over the cam surface. Prepare.

  Example 57-First closure means includes a distal cam surface on a portion of the distal end of the closure member, and second closure means includes a distal cam surface on another portion of the distal end. 57. The surgical tool assembly of example 56, including a distal camming surface extending from the distal cam surface at an obtuse angle to the same.

  Example 58-A cam surface is formed on an anvil mounting portion, the anvils being first and second pivotally mounted to elongate channels, respectively, for selective pivoting about a pivot axis. 58. The surgical tool assembly according to example 56 or 57, further comprising two mounting walls.

  Example 59-A shaft assembly is selectively axially movable between a first mounting wall and a second mounting wall between a start position and an end position. 59. The surgical tool assembly according to embodiment 58, further comprising a flexible firing member.

  Example 60-The surgical tool assembly of example 59, wherein at least a portion of the firing member is proximal of the cam surface when the firing member is in the starting position.

  Example 61-A surgical tool assembly comprising a surgical end effector and a closure member axially movable in response to applied closing and opening movements. The surgical end effector includes a first jaw and a second jaw including a second jaw body portion and a second jaw mounting portion. The second jaw mounting portion is movably connected to the first jaw for selectively moving between the open and closed positions relative to the first jaw. The closure member includes at least one open cam formed thereon, the at least one open cam configured to movably engage a corresponding cam surface formed on the second jaw body portion. As a result, when an opening motion is applied to the closure member, the at least one opening cam movably engages a corresponding cam surface to move the second jaw to the open position. When a closing motion is applied to the closing member, the closing member engages the second jaw to move the second jaw to one of the closed positions.

  Example 62-At least one open cam extends distally from the distal end of the closure member and a camming engagement with a first one of the cam surfaces formed on the second jaw body portion. A first hook portion configured to engage and a second one of the cam surfaces extending distally from the distal end of the closure member and formed on the second jaw body portion. The second embodiment, wherein the second hook portion is configured to be in a camming engagement with a second hook portion.

  Example 63-The surgical tool assembly of examples 61 or 62, wherein the cam surface comprises a downwardly extending beveled surface formed on the second jaw body portion.

  Embodiment 64-An embodiment wherein each of the at least one opening cam comprises a camming end formed thereon configured to come into engagement with a corresponding ramp when an opening motion is applied to the closure member. 63. The surgical tool assembly according to 63.

  Example 65-Each ramp has a ramp end, and each camming end engages the ramp end of the corresponding ramp to fully open the second jaw to the first jaw. 65. The surgical tool assembly according to example 64, configured to hold in position.

  Example 66-The surgical tool of any of Examples 61, 62, 63, 64, or 65, wherein the surgical tool assembly further comprises secondary jaw opening means for applying an additional opening movement to the second jaw. assembly.

  Embodiment 67-The secondary jaw opening means engages a corresponding jaw opening mechanism on said second jaw to apply an additional opening movement to the second jaw when the opening movement is applied to the closing member. 67. The surgical tool assembly according to example 66, comprising at least one secondary jaw opening member on the closure member configured.

  Example 68-A secondary jaw opening mechanism is integrally formed within a closure member and at least one first jaw opening tab configured to contact a corresponding one of the corresponding jaw opening mechanisms And at least one second jaw opening tab integrally formed in the closure member and configured to contact another corresponding one of the corresponding jaw opening mechanisms. 68. The surgical tool assembly according to 67.

  Embodiment 69-A surgical tool according to embodiments 66, 67 or 68, wherein the secondary jaw opening means comprises at least one biasing member configured to apply an additional opening movement to the second jaw. assembly.

  Example 70-The surgical tool assembly of Examples 62, 63, 64, 65, 66, 67, 68, or 69, wherein each of the first and second hook portions includes a flexible portion thereon.

  Example 71-The surgical tool assembly of example 70, wherein the flexible portion includes a flexible material attached to each of the first and second hook portions.

  Embodiment 72-The embodiment 70 or wherein the at least one biasing member comprises a spring corresponding to each of the first and second hook portions and attached to each of the first and second hook portions. 72. The surgical tool assembly according to 71.

  Example 73-A surgical tool assembly comprising a surgical end effector and a closure member axially movable in response to applied closing and opening movements. The surgical end effector includes an elongated channel configured to operatively support a surgical staple cartridge therein, and an anvil comprising an anvil body and an anvil mounting portion, wherein the anvil mounting portion is in an open position and a closed position. A pivotal support is provided on the elongate channel for selective movement with respect to the elongate channel. The closure member includes at least one open cam formed thereon, the at least one open cam being configured to movably engage a corresponding cam surface formed on the anvil body, As a result, when an opening motion is applied to the closing member, the at least one opening cam movably engages a corresponding cam surface to move the anvil to the open position, and when the closing motion is applied to the closing member, The closure member engages the anvil and moves the anvil to one of the closed positions.

  Example 74-The surgical tool assembly of Example 73, further comprising at least one tissue stop formed on the anvil body, wherein at least one cam surface is proximal to the at least one tissue stop. A surgical tool assembly according to claim 1.

  Example 75-At least one open cam extends distally from a distal end of a closure member and engages a first one of the cam surfaces formed on the anvil body. A first hook portion configured and extending distally from the distal end of the closure member and for camming engagement with a second one of the cam surfaces formed on the anvil body. A surgical tool assembly according to example 73 or 74, comprising: a second hook portion configured.

  Example 76-The surgical tool assembly of example 75, wherein the first and second hook portions each include a flexible portion thereon.

  Embodiment 77-The surgical tool assembly of embodiment 73 or 74, wherein the first and second hook portions each include a flexible portion thereon.

  Embodiment 78-The surgical tool of any of embodiments 73, 74, 75, 76, or 77, wherein the surgical tool assembly further comprises a secondary anvil opening means for applying an additional opening motion to the second jaw. assembly.

  Embodiment 79-The embodiment 79 of embodiment 78, wherein the anvil is pivotally connected to the elongate channel for selectively pivoting between an open position and a closed position about a pivot axis. Surgical tool assembly. The secondary anvil opening means is located proximal to the pivot axis.

  Example 80- A surgical tool assembly, comprising a surgical end effector and a closure member. The surgical end effector includes an elongated channel configured to operably support a surgical staple cartridge therein, and an anvil including an anvil body and an anvil mounting portion. An anvil mounting portion is pivotally supported on the elongate channel for selective movement with respect to the elongate channel between an open position and a closed position. The closing member is axially movable between a fully activated position corresponding to the fully closed position of the closed positions and a non-activated position corresponding to the open position. The closure member includes a closure system configured to sequentially apply an initial opening motion to the anvil and an additional secondary motion to the anvil when the closure member is moved from the fully activated position to the inactivated position.

  Example 81-A surgical end effector, wherein a first jaw configured to operably support a surgical staple cartridge therein and for selective movement between an open position and a closed position. A surgical end effector, comprising: a second jaw movably supported relative to the first jaw; a firing member; and a firing member lockout system. The firing member is supported to move axially within the first jaw along the shaft axis between a start position and an end position when the firing and retraction motions are applied. The firing member lockout system is movable between the inactive position and the locked position by the second jaw, and is positioned in the unfired position when the firing member is first advanced distally from the starting position. As long as the unfired surgical staple cartridge with the cam assembly is not supported in the first jaw, the firing member will have a firing member lockout system and a locking member to prevent further distal advancement of the firing member. Combine.

  Example 82-The surgical end effector of Example 81, wherein the firing member lockout system comprises a locking member mounted on the first jaw.

  Embodiment 83- The surgical procedure of embodiment 82, wherein the locking member further comprises a spring tab configured to support the locking member on the first jaw and bias the locking member to the unlocked position. End effector.

  Example 84-The locking member is activated during the first distal advance of the firing member when the second jaw is in the closed position unless the unfired surgical staple cartridge is supported within the first jaw. 84. The surgical end effector of any of embodiments 82 or 83, comprising at least one laterally movable locking portion configured to lockly engage a portion of the surgical end effector.

  Example 85-A firing member comprises a firing member body having a lock protrusion corresponding to each of the laterally movable lock portions, each lock protrusion having an unfired surgical staple cartridge supported in a first jaw. 85. The method of embodiment 84, wherein the second jaw is oriented to lockly engage with the corresponding laterally movable lock portion upon initial distal advancement of the firing member when in the closed position unless otherwise. Surgical end effector.

  Embodiment 86-A cam assembly includes an unfired surgical staple cartridge supported in a first jaw and laterally applying each of the corresponding laterally movable locking portions when the cam assembly is in the unfired position. 86. The surgical end effector according to embodiment 85, comprising an unlocking mechanism corresponding to each laterally movable lock portion for biasing and releasing the lock engagement with the corresponding lock protrusion.

  Embodiment 87-Each of the laterally movable locking portions includes a locking window configured to lockly receive a portion of the corresponding locking projection when the laterally movable locking portion is in locking engagement with the corresponding locking projection. 87. The surgical end effector according to example 85 or 86, comprising:

  Embodiment 88-The firing member lockout system moves to the second jaw to move along a corresponding lock axis transverse to the shaft axis when the anvil is in the closed position. 88. The surgical end effector according to any of embodiments 81, 82, 83, 84, 85, 86, or 87, comprising at least one locking member operatively connected.

  Example 89-A firing member lockout system includes a locking member movably supported to move between an unlocked position and a locked position, wherein upon initial firing of the firing member, the locking member Examples 81, 82, 83, wherein at least a portion of is configured to hook engage a corresponding portion of the firing member to prevent the firing member from advancing from a start position to an end position. 84. The surgical end effector according to 84, 85, 86, 87 or 88.

  Example 90-A surgical end effector, wherein an elongate channel configured to operably support a surgical staple cartridge therein and an anvil, wherein the anvil is in an open position and a closed position relative to the elongate channel. A surgical end effector comprising an anvil supported relative to an elongate channel, a firing member, and a firing member lockout system so as to be selectively movable between the firing member and a firing member. The firing member is supported to move axially along the shaft axis between a start position and an end position within the elongate channel when the firing and retraction motions are applied. The firing member lockout system is movable between an inactive position and a locked position by the anvil, such that when the firing member is first advanced distally from the starting position, the firing member is positioned in the unfired position. Lock engagement with a firing member lockout system to prevent further distal advancement of the firing member unless an unfired surgical staple cartridge with a moving cam assembly is supported within the elongate channel. The firing member lockout system is configured to move from the inactive position to the locked position when the anvil is moved to the closed position.

  Example 91-The surgical end effector according to example 90, wherein the firing member lockout system comprises a locking member. The locking member includes a pair of laterally movable locking portions, a mounting portion configured to support the locking member on the surgical end effector and to bias the locking member to the inoperative position, and the anvil to the closed position. At least one anvil tab on the locking member for contacting by a corresponding portion of the anvil when being moved.

  Example 92-Each laterally movable locking portion retains a corresponding portion of the firing member when the locking member is in the locked position unless the unfired surgical staple cartridge is supported in the elongate channel. 90. The surgical end effector according to example 91, comprising a locking window configured to engage.

  Embodiment 93-Each corresponding portion of a firing member corresponds to a respective one of the locking windows of a corresponding laterally movable locking portion and includes an unfired surgical staple cartridge with a cam assembly located in an unfired position. Is sized to be resiliently received within each of the locking windows in lock engagement with each of the locking windows when the locking member is in the locked position, unless supported within the elongate channel. The surgical end effector of example 92, comprising a laterally projecting locking lug.

  Example 94-A cam assembly laterally biases each of the corresponding laterally movable locking portions when an unfired surgical staple cartridge is supported in the elongated channel and the cam assembly is in the unfired position. 94. The surgical end effector of embodiment 93, further comprising an unlocking mechanism corresponding to each laterally movable lock portion to disengage lock engagement with a corresponding lock lug.

  Example 95-A firing member lockout system comprises at least one locking member, wherein the anvil comprises an anvil body and an anvil mounting portion comprising a pair of spaced anvil mounting walls, each anvil mounting wall comprising: Examples 90, 91, 92, 93, or 94, wherein each anvil mounting wall is pivotally supported on an elongate channel and each anvil mounting wall movably supports a corresponding one of the locking members therein. A surgical end effector as described.

  Example 96-A firing member lockout system includes at least one locking member movably coupled to an anvil for movement along a corresponding locking axis transverse to a shaft axis when the anvil is in a closed position. The surgical end effector according to any of embodiments 90, 91, 92, 93, 94, or 95, comprising:

  Example 97-The surgical end effector of any one of Examples 90, 91, 92, 93, 94, 95, or 96, wherein the surgical end effector further comprises a tissue cutting surface on the firing member.

  Example 98-A surgical instrument comprising: an elongate shaft defining a shaft axis; an elongate channel operably coupled to the elongate shaft and configured to operably support a surgical staple cartridge therein. An anvil supported with respect to the elongated channel such that the anvil is selectively movable between an open position and a closed position with respect to the elongated channel. The surgical instrument includes a firing member supported to move axially between a start position and an end position within the elongate channel when the firing and retraction motions are applied; and Means for preventing the firing member from moving from the start position to the end position unless the unfired surgical staple cartridge with the cam assembly located in the unfired position is supported in the elongated channel; Is further provided.

  Example 99-The surgical instrument of example 98, wherein the anvil comprises an anvil body and a pair of anvil mounting walls extending from the anvil body. Each anvil mounting wall is such that the anvil can be selectively moved between an open position and a closed position relative to the elongate channel when a closing and opening motion is applied to the anvil by the closed portion of the elongate shaft assembly. And is pivotally connected to the elongate channel.

  Embodiment 100-The means for preventing is a lock member movably supported to move between an unlocked position and a locked position, at least in part where the firing member is in the starting position. And a locking member configured to hook into a corresponding portion of the firing member to prevent advancement from a forward position to an end position; and a biasing member for biasing the firing member to an unlocked position. A surgical instrument according to any of embodiments 98 or 99, comprising:

  Example 101-A surgical instrument comprising a surgical end effector, an elongate shaft defining a shaft axis, a closure member, and an articulation. The surgical end effector includes a first jaw and a second jaw movably supported on the first jaw for selectively moving between an open position and a closed position with respect to the first jaw. Joe (just). The closure member is movably supported on the elongate shaft and is configured to selectively move in an opening direction from an open position to a closed position and in an open direction from a closed position to an open position. The articulation couples the surgical end effector to the elongate shaft such that the surgical end effector is selectively articulatable relative to the elongate shaft about an articulation axis transverse to the shaft axis. The articulation is a locked configuration in which the surgical end effector is prevented from articulating about the articulation axis, and an unlocked configuration in which the surgical end effector is articulable about the articulation axis. An articulation locking mechanism configured to move from the configuration. The joint locking mechanism moves from the locked configuration to the unlocked configuration when the closing member is moved from the open position in the closing direction. The surgical instrument further comprises means for applying articulation to the surgical end effector when the joint locking mechanism is in the unlocked configuration.

  Example 102-An articulated locking mechanism comprises at least one locking member, wherein at least one locking member has a first position corresponding to an unlocked configuration, and at least one locking member has a surgical end effector mounted thereon. 102. The surgical instrument of embodiment 101, wherein the surgical instrument is movable between a portion and a second position that frictionally engages a distal end portion of the elongate shaft. The at least one locking member operably interfaces with the closing member such that initial movement of the closing member in the closing direction moves the at least one locking member from the first position to the second position.

  Example 103-The surgical end effector of claim 102, wherein the mounting portion of the surgical end effector comprises an upright mounting column including a plurality of column sides, and wherein at least one locking member comprises a locking member corresponding to each of the column sides. Surgical instruments.

  Example 104-The distal end portion of the elongate shaft includes a pivot hole that defines an articulation axis, and the upright mounting column extends into the pivot hole so that each of the locking members is within the pivot hole. 104. The surgical instrument of embodiment 103, wherein the surgical instrument is movably supported between a corresponding column side and an inner wall of the pivot hole.

  Example 105-An upright mounted column is configured to move a plurality of locking members into frictional engagement with the inner wall of a pivot hole and corresponding column sides when the closing member is moved in a closing direction. The surgical instrument according to Example 104.

  Example 106-Closure Member Interfacing with Sources of Closure and Opening Motion to Move Proximal Closure in Closing and Opening Directions, and Pivot to Proximal Closure by Linking Mechanism And a portion of the linkage mechanism interfacing with the upright mounting column such that when the closing member is first moved in the closing direction, the upright mounting column includes a plurality of locking members. 108. The surgical instrument of example 105, wherein the surgical instrument is configured to move the inner surface of the pivot hole into frictional engagement with the inner wall of the pivot hole and the corresponding column side wall.

  Example 107-A link mechanism is pivotally connected to and extends between a proximal closure member and a distal closure member, an upper double pivot link, and a proximal closure member and a distal closure member. 107. The surgical instrument of example 106, comprising a lower dual pivot link pivotally coupled to the member and extending therebetween. The lower double pivot link is configured to operably interface with the upright mounting column to apply a locking motion to the upright mounting column when the lower double pivot link is first moved in the closing direction. .

  Example 108-An upright mounting column comprises a first end mounted to a mounting base adjacent a lower double pivot link, the upright column tapering toward a free end, 108. The surgical instrument of embodiment 107, wherein the cross-sectional area of the end is less than another cross-sectional area of the first end of the column.

  Example 109-Examples 101, 102, 103, 104 wherein a first jaw comprises an elongated channel configured to operatively support a surgical staple cartridge therein and a second jaw comprises an anvil. 108, 105, 106, 107, or 108.

  Example 110-Means for applying articulation to a surgical end effector comprises applying a first articulation to the surgical end effector and applying the surgical end effector in a first articulation direction about the articulation axis. Means for articulating and means for applying the second articulation to the surgical end effector and articulating the surgical end effector in a second articulation direction about the articulation axis. Surgical instrument according to any of claims 101, 102, 103, 104, 105, 106, 107, 108 or 109.

  Example 111-A surgical instrument comprising: an elongate shaft having a distal end portion and defining a shaft axis; a surgical end effector; an articulating locking mechanism; and an articulating member. . The surgical end effector includes an end effector mounting portion, the distal end portion of the elongate shaft and one of the end effector mounting portions includes a pivot hole, and the distal end portion of the elongate shaft and the other of the end effector mounting portion include: A surgical end effector is pivotally received within the pivot hole to define an articulation axis transverse to the shaft axis, and about the shaft axis, the surgical end effector transfers the articulation to the surgical end effector. In addition, it is articulatable with respect to the elongate shaft. The joint locking mechanism is supported in the pivot hole between the articulation pin and the inner wall of the pivot hole. The articulation locking mechanism is a first locked mechanism wherein the articulation locking mechanism frictionally engages the articulation pin and the inner wall of the pivot hole to prevent relative pivotal movement of the articulation pin and the distal end portion of the elongated shaft. And an unlocked configuration in which the articulation pin and the distal end portion are pivotable with respect to each other. The articulation member interfaces with the surgical end effector such that actuation of the articulation member causes the articulation member to apply articulation to the surgical end effector. The articulation member moves from the locked configuration to the unlocked configuration by the initial operation of the articulation member, and when the articulation member is stopped, the articulation member shifts from the unlocked configuration. Interfaces with the joint locking mechanism to move to the locked configuration.

  Example 112-The surgical instrument of Example 111, wherein the articulation locking mechanism comprises a torsion spring supported between the articulation pin and the inner wall of the pivot hole.

  Example 113-A torsion spring is a first torsion spring that frictionally engages an articulation pin and an inner wall of a pivot hole to prevent relative pivotal movement of a distal end portion of an elongate shaft and a surgical end effector. 112. The surgical instrument of embodiment 112, wherein the surgical instrument is rotatable from a position and a position where the torsion spring does not prevent relative pivotal movement.

  Example 114-An articulating locking mechanism comprises at least one locking ball, wherein at least one locking ball is between an articulating pin and an inner wall of a pivot hole, each locking ball being between an articulating pin and an inner wall of the pivot hole. A first position that frictionally engages the distal end portion of the elongate shaft and the relative pivotal movement of the surgical end effector, and a position where each of the locking balls does not prevent the relative pivotal movement. 114. The surgical instrument according to any of examples 111, 112, or 113, comprising at least one locking ball movably supported between and.

  Example 115-The surgical end effector according to any of Examples 111, 112, 113, or 114, comprising a first jaw and a second jaw supported for movable movement relative to the first jaw. Surgical instruments.

  Example 116-The surgical instrument of Example 115, wherein the first jaw comprises an elongated channel configured to operatively support a surgical staple cartridge therein and the second jaw comprises an anvil. .

  Example 117-An articulating member comprises an axially movable articulating member pivotally connected to a surgical end effector such that its axial movement in a first axial direction comprises: The surgical end effector is articulated in a first articulation direction about an articulation axis, and movement of the axially movable articulation member in a second axial direction causes the surgical end effector to articulate the surgical end effector. 118. The surgical instrument of any of examples 111, 112, 113, 114, 115, or 116, wherein the surgical instrument is articulated about a movement axis in a second articulation direction.

  Example 118-A surgical instrument comprising a surgical end effector, an elongate shaft defining a shaft axis, closure means, and an articulation. The surgical end effector includes a first jaw movably connected to the elongate shaft for selectively articulating relative to the elongate shaft about an articulation axis transverse to the shaft axis, and a first jaw coupled to the first jaw. A second jaw movably supported on the first jaw to selectively move between an open position and a closed position. The closing means is further configured to selectively move the second jaw from the open position to the closed position, and the closing means is further configured to selectively move the second jaw from the closed position to the open position. . The articulation connects the surgical end effector to the elongate shaft such that the surgical end effector is selectively articulatable relative to the elongate shaft about an articulation axis transverse to the shaft axis. The articulation is a locked configuration in which the surgical end effector is prevented from articulating about the articulation axis, and an unlocked configuration in which the surgical end effector is articulable about the articulation axis. An articulation locking mechanism configured to move from the configuration. The joint locking mechanism moves from the locked configuration to the unlocked configuration when the closing means moves the second jaw from the open position to the closed position. The surgical instrument further comprises means for applying articulation to the surgical end effector when the joint locking mechanism is in the unlocked configuration.

  Example 119-The surgical instrument of Example 118, wherein the first jaw comprises an elongated channel configured to operably support a surgical staple cartridge therein and the second jaw comprises an anvil. .

  Example 120-An articulated locking mechanism comprises at least one locking member, wherein at least one locking member has a first position corresponding to an unlocked configuration and at least one locking member has a first jaw mounted. 121. The surgical instrument according to example 119 or 120, wherein the surgical instrument is movable between a portion and a second position that frictionally engages a distal end portion of the elongate shaft. The at least one locking member operably interfaces with the closing member such that initial movement of the closing member in the closing direction moves the at least one locking member from the first position to the second position.

  Example 121-A surgical instrument, comprising an elongate shaft defining a shaft axis, a surgical end effector, at least one articulation link, and an articulation locking mechanism. The surgical end effector is coupled to the elongate shaft for selective articulation relative to the elongate shaft about an articulation axis transverse to the shaft axis. At least one articulation link is operatively interfaced with the articulation source and coupled to the surgical end effector for applying articulation to the surgical end effector. The articulation locking mechanism includes articulation locking members corresponding to each articulation link, each articulation locking member moving laterally from an unlocked position laterally adjacent to the corresponding articulation link to correspond to the articulation link. It is configured to lock-engage with the articulation link. The surgical instrument is operatively interfaced with each of the articulation locking members to selectively laterally move each of the articulation locking members from an unlocked position to lock and engage a corresponding articulation link. Means are further provided.

  Example 122-Each at least one articulation link comprises an articulation gear rack, an articulation lock corresponding to each articulation gear rack, and a corresponding articulation lock facing the articulation link. Example 121, comprising a locking gear rack that is oriented with respect to each articulating gear rack in a lateral, face-to-face relationship for mating engagement with each articulating gear rack when advanced laterally. Surgical instruments.

  Example 123-At least one articulation link includes an axially movable right articulation link including a right articulation gear rack above and an axially movable left articulation including a left articulation gear rack above The surgical instrument of any of embodiments 121-122, comprising: a motion link. The articulation lock member is a right lock that is in a laterally facing relationship with the right articulation gear rack for mating engagement with the right articulation gear rack when the right articulation lock member is advanced laterally toward the right articulation link. A right articulating locking member including a gear rack, and a lateral facing relationship with the left articulating gear rack for mating engagement with the left articulating gear rack when the left articulating lock member is advanced laterally toward the left articulating link. And a left joint lock member including a left lock gear rack.

  Embodiment 124-The actuating means comprises a lock actuator movably positioned relative to the right and left joint locking members, thereby moving the lock actuator axially in the first axial direction. The right articulation lock member is moved laterally toward the right articulation link, thereby locking the right lock gear rack with the right articulation gear rack, and the left articulation lock member is laterally moved toward the left articulation link. 124. The surgical instrument of example 123, wherein the left locking gear rack is brought into lock engagement with the left articulating gear rack.

  Example 125-A source of articulating motion includes an axially movable firing actuator and an axially movable firing configured to selectively apply a firing motion to a corresponding portion of a surgical end effector. An actuator and an articulation transmitter operably interfaced with the at least one articulation link, whereby actuation of the axially movable firing actuator in the first axial firing direction comprises at least one Movement of the articulation link in a first axial articulation direction and movement of the axially movable firing actuator in a second axial retraction direction causes the at least one articulation link to move in the second axial direction. 125. The surgical instrument of any of Examples 121, 122, 123, or 124, wherein the surgical instrument is moved in a direction of articulation.

  Example 126-A source of articulation includes an axially movable firing actuator configured to selectively apply a firing motion to a corresponding portion of a surgical end effector, a right articulation link and a left joint. An articulation transmitter operably interfaced with the motion link and the axially movable firing member, whereby actuation of the axially movable firing actuator in the first axial firing direction comprises: The right articulation link is moved in the first axial direction, the left articulation link is moved in the second axial direction, and the movement of the axially movable firing actuator in the second axial direction is performed by the right articulation link. 124. The surgical instrument of example 123 or 124, wherein is moved in a second axial direction and the left articulation link is moved in a first axial direction.

  Embodiment 127-The articulation locking mechanism further comprises a lock actuator movably positioned relative to the articulation locking member and the left articulation locking member, such that axial movement of the lock actuator in the first axial direction is to the right. The articulation locking member is moved laterally toward the right articulation link, thereby locking the right locking gear rack with the right articulation gear rack and the left articulation locking member is laterally moving toward the left articulation link. 127. The surgical instrument of example 126, wherein the surgical instrument is moved to thereby lock the left locking gear with the left articulating gear rack.

  Example 128-An articulation transmitter is configured to selectively mesh with a gear assembly that meshes with a right articulation link and a left articulation link, and with a gear assembly and an axially movable firing actuator. 127. The surgical instrument of example 127, comprising: a shifted shifter. The shifter is configured to selectively operably engage with the lock actuator, such that when the shifter is operatively engaged with the lock actuator, the shifter is moved to provide an axially movable firing. Engagement with the actuator and gear assembly and movement of the shifter out of operable engagement with the lock actuator further moves the shifter into engagement with the gear assembly and the axially movable firing actuator. Get out of engagement.

  Example 129-The surgical instrument of Example 125, wherein the corresponding portion of the surgical end effector comprises a firing member mounted on an axially movable firing actuator. The firing member is supported for axial movement through the surgical end effector between a start position and an end position within the surgical end effector.

  Example 130-A surgical instrument, comprising: an elongate shaft defining a shaft axis; a surgical end effector; a firing actuator; and at least one configured to selectively operably engage the firing actuator. A surgical instrument comprising an articulation link and an articulation locking mechanism. The surgical end effector is coupled to the elongate shaft for selective articulation relative to the elongate shaft about an articulation axis transverse to the shaft axis. The firing actuator is selectively axially movable in first and second axial directions to apply a firing motion to a firing member operably supported within the surgical end effector. The axial movement of the firing actuator is transmitted to each of the at least one articulation link. The articulation locking mechanism includes a locked configuration in which each of the at least one articulation link is immovably locked in place and each of the at least one articulation link is responsive to movement of the firing actuator. It is configured to move laterally between a movable, unlocked configuration. The articulation locking mechanism is configured to operatively engage the firing actuator with each of the at least one articulation link when the articulation locking mechanism is in the unlocked configuration and to at least when the articulation locking mechanism is in the locked configuration. Interface with the firing actuator such that each of the one articulation link is prevented from operatively engaging the firing actuator.

  Example 131-The surgical instrument of example 130, wherein the articulation locking mechanism comprises an articulation lock member corresponding to each articulation link. Each articulation locking member is configured to move laterally from an unlocked position laterally adjacent to a corresponding articulation link and lock-engage with the corresponding articulation link.

  Embodiment 132-Each at least one articulation link comprises an articulation gear rack, and each corresponding articulation lock member has a corresponding articulation when the articulation lock member is advanced laterally toward the corresponding articulation link. A locking gear rack oriented to the articulation gear rack of the corresponding articulation link in a lateral facing relationship to the articulation gear rack of the corresponding articulation link for mating engagement with the articulation gear rack of the link; The surgical instrument according to Example 131.

  Example 133 At least one articulation link includes an axially movable right articulation link including a right articulation gear rack above, and an axially movable left articulation link including a left articulation gear rack above 135. The surgical instrument of example 132, comprising: a motion link. The articulation lock member is a right lock that is in a laterally facing relationship with the right articulation gear rack for mating engagement with the right articulation gear rack when the right articulation lock member is advanced laterally toward the right articulation link. A right articulating locking member including a gear rack, and a lateral facing relationship with the left articulating gear rack for mating engagement with the left articulating gear rack when the left articulating lock member is advanced laterally toward the left articulating link. And a left joint lock member including a left lock gear rack.

  Example 134-The surgical end effector according to any of Examples 130, 131, 132, or 133 comprising a firing member coupled to the firing actuator and supported for axial movement through the surgical end effector. The surgical instrument as described.

  Example 135-A surgical end effector includes an elongate channel configured to operably support a surgical staple cartridge therein, and an elongate channel for selectively moving between an open position and a closed position. 138. The surgical instrument of embodiment 134 comprising a movably supported anvil. The elongate channel is coupled to the elongate shaft for selective articulation relative to the elongate shaft about an articulation axis. The firing member includes a tissue cutting mechanism.

  Example 136-A surgical instrument further comprises an articulation transmitter operably interfaced with a right articulation link and a left articulation link and an axially movable firing actuator, thereby enabling axial movement. Actuation of the firing actuator in a first axial firing direction includes moving the right articulation link in the first axis direction, moving the left articulation link in the second axis direction, and axially movable firing. 135. The surgical instrument of example 133 wherein movement of the actuator in the second axial direction causes the right articulation link to move in the second axial direction and the left articulation link to move in the first axial direction.

  Example 137-The joint locking mechanism further comprises a lock actuator movably positioned with respect to the right and left joint locking members, such that axial movement of the lock actuator in the first axial direction is The right articulation lock member is moved laterally toward the right articulation link, thereby locking the right lock gear rack with the right articulation gear rack, and the left articulation lock member is laterally moved toward the left articulation link. 136, wherein the left locking gear is in lock engagement with the left articulating gear rack.

  Example 138-Articulation transmitter is configured to selectively mesh with a gear assembly that meshes with a right articulation link and a left articulation link, and an axially movable firing actuator. 136. The surgical instrument of example 136 comprising: The shifter is configured to selectively operably engage with the lock actuator, such that when the shifter is operatively engaged with the lock actuator, the shifter is moved to provide an axially movable firing. It is in meshing engagement with the actuator and gear assembly. When the shifter is out of operable engagement with the lock actuator, the shifter is moved out of meshing engagement with the gear assembly and the axially movable firing actuator.

  Example 139-A surgical instrument coupled to an elongate shaft that defines a shaft axis and selectively articulates relative to the elongate shaft about an articulation axis transverse to the shaft axis. A surgical instrument comprising a surgical end effector, means for generating an axial firing motion, and articulation means. The articulation means interfaces with the means for producing, the articulation means responsive to the axial firing movement produced by the means for producing to apply articulation to the surgical end effector. Is configured. The surgical instrument selectively locks the articulation means in a non-movable configuration and unlocks the articulation means, such that the means for generating can apply an axial firing movement to the articulation means. Means for operatively coupling the articulating means and the means for generating are further provided.

  Example 140-A surgical end effector includes an elongate channel configured to operably support a surgical staple cartridge therein, and an elongate channel for selectively moving between an open position and a closed position. 139. The surgical instrument of embodiment 139 comprising: an anvil movably supported on the surgical instrument. The elongate channel is coupled to the elongate shaft for selective articulation relative to the elongate shaft about an articulation axis. The firing member includes a tissue cutting mechanism.

  Example 141-A surgical tool assembly coupled to an elongate shaft defining a shaft axis and selectively articulating relative to the elongate shaft about an articulation axis transverse to the shaft axis. A surgical end effector, a first articulation link, a second articulation link, and an articulation stroke amplifier. The first articulation link is operably interfaced with a source of articulation to selectively axially move the first articulation link in a first articulation direction by a first axial distance. I do. The second articulation link operably interfaces with the surgical end effector to apply articulation to the surgical end effector. The articulation stroke amplifier is configured to move the second articulation link to the first articulation link when the first articulation link is axially moved in the first axial direction by a first axial distance. Operatively interface with the first articulation link and the second articulation link to move axially by another first axial distance greater than the first axial distance.

  Example 142-A source of articulation is configured to additionally axially move a first articulation link in a second axial direction by a second axial distance. Is moved in the second axial direction by a second axial distance, the articulation stroke amplifier causes the second articulation link to move in the second axial direction to another, larger than the second axial distance. 142. The surgical tool assembly according to example 141, wherein the surgical tool assembly is moved by a second axial distance.

  Example 143-A first articulation link comprises a first articulation gear rack, a second articulation link comprises a second articulation gear rack, and the articulation stroke amplifier comprises first and second articulations. 144. The surgical tool assembly according to example 141 or 142, comprising at least one gear set for meshing engagement with a gear rack.

  Example 144-Each at least one gearset is rotatably supported in mesh with a first articulating gear rack and a first gear rotatably supported in meshing engagement with a first articulating gear rack. 143. The surgical tool assembly according to example 143, comprising: a first gear supported on the first gear.

  Embodiment 145-The surgical tool of any of embodiments 141, 142, 143, or 144, wherein the second articulation link operably interfaces with an articulation lock assembly operably connected to the surgical end effector. assembly.

  Example 146-A first articulation link comprises a first articulation gear rack and an articulation stroke amplifier is in meshing engagement with the first articulation gear rack and is slidable on the second articulation link. 153. The surgical tool assembly according to any one of Examples 141, 142, 143, 144, or 145, comprising a coupled swing gear.

  Example 147-Example 141, 142, 143, 144, 145, or wherein the swing gear is supported for rotational movement about a swing gear mounting axis that traverses the first and second articulation links. 146. The surgical tool assembly according to 146.

  Example 148-The surgical tool assembly of Examples 146 or 147, wherein the second articulation link comprises a slotted distal end slidably engaging a portion of the swing gear therein.

  Example 149-An embodiment 146, 147, or 148, wherein the swing gear has a slot configured therein to slidably engage a distal end portion of the second articulation link. Surgical tool assembly.

  Example 150-A surgical tool assembly, comprising: an elongate shaft defining a shaft axis, a surgical end effector, a first articulation link, a second articulation link, and an articulation stroke amplifier. A surgical tool assembly comprising: The surgical end effector is configured to operably support a surgical staple cartridge therein, and the surgical end effector is configured to selectively articulate relative to the elongate shaft about an articulation axis transverse to the shaft axis. An elongate channel is coupled and an anvil movably supported on the elongate channel. The first articulation link is operably interfaced with a source of articulation to selectively axially move the first articulation link in a first articulation direction by a first axial distance. I do. The second articulation link operably interfaces with the surgical end effector to apply articulation to the surgical end effector. The articulation stroke amplifier is configured such that when the first articulation link is axially moved in the first axial direction by a first axial distance, the articulation stroke amplifier switches the second articulation link to the first articulation link. Operably interface with the first articulation link and the second articulation link to move in the first axial direction by another first axial distance that is greater than the first axial distance.

  Example 151-A source of articulation includes a firing member assembly operatively interfaced with a firing member supported to move axially within an elongated channel, a first articulation link and firing member assembly, Operatively interfacing between a firing mode in which axial movement of the firing member assembly is applied to the firing member and an articulation mode in which axial movement of the firing member assembly is applied to the first articulation link. 160. The surgical tool assembly according to example 150, comprising a clutch assembly, which is selectively configurable at.

  Example 152-When the clutch assembly is in an articulation mode, the firing member assembly is configured to additionally axially move the first articulation link in a second axial direction by a second axial distance. And when the first articulation link is moved in the second axial direction by a second axial distance, the articulation stroke amplifier moves the second articulation link in the second axial direction to the second axial direction. The surgical tool assembly of example 151, wherein the surgical tool assembly is moved by another second axial distance that is greater than the axial distance.

  Example 153-A first articulation link comprises a first articulation gear rack, a second articulation link comprises a second articulation gear rack, and the articulation stroke amplifier comprises a first and a second articulation. 153. The surgical tool assembly according to example 151 or 152, comprising at least one gear set for meshing engagement with a gear rack.

  Example 154-Each at least one gear set includes a first gear rotatably supported in meshing engagement with a first articulating gear rack and a first gear for rotation with the first gear. 153. The surgical tool assembly of example 153, comprising: a second gear attached. The second gear has a diameter greater than the diameter of the first gear, and the second gear is in meshing engagement with a second articulating gear rack.

  Embodiment 155-The surgical tool of any of embodiments 151, 152, 153, or 154, wherein the second articulation link operably interfaces with an articulation lock assembly operably coupled to the surgical end effector. assembly.

  Example 156-A first articulation link comprises a first articulation gear rack, and an articulation stroke amplifier is in meshing engagement with the first articulation gear rack and is slidable on the second articulation link. 160. The surgical tool assembly according to any of the embodiments 151, 152, 153, 154, or 155, comprising a coupled swing gear.

  Example 157-The surgical tool assembly of Example 156, wherein the swing gear is supported for rotational movement about a swing gear mounting axis that traverses the first and second articulation links.

  Example 158-The surgical tool assembly of Examples 156 or 157, wherein the second articulation link comprises a slotted distal end slidably engaging a portion of the swing gear therein.

  Example 159-An embodiment 156, 157, or 158, wherein the swing gear has a slot configured therein to slidably engage a distal end portion of the second articulation link. Surgical tool assembly.

  Example 160-A surgical tool assembly, comprising: an elongated shaft defining a shaft axis; a surgical end effector; a first articulation link; a second articulation link; A surgical tool assembly comprising: The surgical end effector is coupled to the elongate shaft for selective articulation relative to the elongate shaft about an articulation axis transverse to the shaft axis. The first articulation link is operably interfaced with a source of articulation to selectively axially move the first articulation link in a first articulation direction by a first axial distance. I do. The second articulation link operably interfaces with the surgical end effector to apply articulation to the surgical end effector. The articulation stroke amplifying means is responsive to the movement of the first articulation link by a first axial distance less than the second axial distance to effect a second articulation of the second articulation. Operably interface with the first articulation link and the second articulation link to move by an axial distance of.

  Example 161-A surgical tool assembly comprising: an elongated shaft assembly defining a shaft axis; a surgical end effector; and a distal articulation member. The surgical end effector is movably connected to the elongate shaft assembly by a distal support link, and the distal support link is pivotally connected to the surgical end effector to define an articulation axis transverse to the shaft axis. I do. The distal support link is pivotally and axially movably coupled to the elongate shaft assembly such that the surgical end effector is in a first non-articulating position aligned with the elongate shaft assembly along the shaft axis. Facilitating selective articulation of the surgical end effector about the articulation axis relative to the elongate shaft assembly between a position and an articulation position located on one side of the shaft axis. The distal articulation member is operably interfaced with a source of articulation and is pivotally connected to the surgical end effector to apply articulation to the surgical end effector.

  Example 162-A distal articulation member is configured to move axially on one side of a shaft axis in response to an applied articulation, and the distal support link is elongated along the shaft axis. 161. The surgical tool assembly of example 161 configured to move axially relative to the shaft assembly.

  Example 163-A distal support link is attached to a distal end pivotally connected to a surgical end effector for pivoting about an articulation axis and to a distal end of an elongate shaft assembly. 162. The surgical tool assembly of example 161 or 162, wherein the proximal end comprises a proximal axial slot configured to receive a corresponding articulation pin therein.

  Example 164-A surgical tool assembly is operably coupled to a proximal articulation member operably interfaced with a source of articulation, and to proximal ends of the proximal articulation member and the distal articulation member. The surgical tool assembly of any of embodiments 161, 162, or 163, further comprising: an articulation lock assembly for selectively locking the distal articulation member to an axial position.

  Example 165-The surgical tool assembly of Example 164, wherein the proximal end of the distal articulation member is pivotally connected to the articulation lock assembly.

  Example 166-The surgical device of any of Examples 161, 162, 163, 164, or 165, wherein the distal support link is pivotally and axially movably coupled to the distal spine member of the elongate shaft assembly. Tool assembly.

  Example 167-A surgical end effector selectively moves relative to an elongate channel between an open position and a closed position, the elongate channel configured to operatively support a surgical staple cartridge therein. 161, 162, 163, 164, 165, or 166, comprising: an anvil movably supported on the elongate channel to perform the operation.

  Example 168-The surgical tool assembly of Example 167, wherein the elongate channel is pivotally connected to the distal support link by an end effector mounting assembly connected to the elongate channel.

  Example 169-A distal articulating member is configured to move axially in first and second axial directions so that when the distal articulating member is moved in a first axial direction, The end effector is articulated in a first articulation direction from a first non-articulated position to any one of the articulated positions, and the distal articulation member is axially moved in a second axial direction. When moved, the surgical end effector is moved in a second articulation direction from any one of the articulation positions to a first non-articulation position, examples 161, 162, 163. 170. The surgical tool assembly according to claim 164, 165, 166, 167, or 168.

  Example 170-A surgical tool assembly for a surgical tool in a second articulation direction beyond a first non-articulated position as the distal articulation member is moved in a second axial direction. The surgical tool assembly according to embodiment 169, further comprising means for preventing movement of the end effector.

  Example 171-A surgical tool assembly comprising an elongate shaft assembly defining a shaft axis, a surgical end effector, a distal support link, and a distal articulation member. The surgical end effector includes an elongated channel configured to operatively support a surgical staple cartridge therein, and an anvil supported for movable movement relative to the surgical staple cartridge. The distal support link is pivotally connected to the elongate channel to define an articulation axis that traverses the shaft axis about which the elongate channel articulates relative to the elongate shaft assembly. obtain. A distal support link is attached to the distal end of the elongate shaft assembly for axial and pivotal movement along the shaft axis relative to the distal end of the elongate shaft assembly. A distal articulation member is supported for axial movement on one side of the shaft axis, and the distal articulation member is pivotally coupled to the elongate channel and is operable with a source of articulation. Interface to

  Example 172-The proximal end of a distal support link has a proximal axial slot configured to receive a corresponding articulation pin mounted on the distal end of the elongate shaft assembly described above. 182. The surgical tool assembly according to embodiment 171, comprising:

  Example 173-A surgical tool assembly is operably coupled to a proximal articulation member operably interfaced with a source of articulation and to proximal ends of the proximal articulation member and the distal articulation member. 171. The surgical tool assembly of example 171 or 172, further comprising: an articulation lock assembly for selectively locking the distal articulation member to an axial position.

  Example 174-The surgical tool assembly of example 173, wherein the proximal end of the distal articulation member is pivotally connected to the articulation lock assembly.

  Example 175-The surgical tool of any of Examples 171, 172, 173, or 174, wherein the distal support link is pivotally and axially movably coupled to the distal spine member of the elongate shaft assembly. assembly.

  Example 176-A distal articulation member is configured to move in a first and second axial direction so that when the distal articulation member is moved in a first axial direction, the surgical end The effector is articulated in a first articulation direction from a first non-articulated position to any one of the articulated positions, and when the distal articulation member is moved in a second axial direction. The embodiment 171, 172, 173, 174, or wherein the surgical end effector has been moved in a second articulation direction from any one of the articulation positions to a first non-articulation position. 175. The surgical tool assembly according to 175.

  Example 177-A surgical tool assembly for a surgical tool in a second articulation direction beyond a first non-articulated position when the distal articulation member is moved in a second axial direction. 177. The surgical tool assembly according to example 176, further comprising means for preventing movement of the end effector.

  Example 178-A surgical tool assembly, comprising: an elongate shaft assembly defining a shaft axis; and means for coupling a surgical end effector to a distal end of the elongate shaft assembly, thereby comprising a surgical end. The effector has a non-articulated position where the surgical end effector is aligned with the elongate shaft along the shaft axis about an articulation axis transverse to the shaft axis, and a joint located on one side of the shaft axis. Means for coupling the surgical end effector to the distal end of the elongate shaft assembly, and means for applying articulation to the surgical end effector, wherein the means may be selectively articulated between an exercise position. A surgical tool assembly comprising: The means for coupling is coupled to the elongate shaft assembly for axial movement and pivotal movement relative to the elongate shaft assembly.

  Embodiment 179-The surgical tool assembly of embodiment 178, wherein the means for adding is pivotally connected to the surgical end effector at a location laterally offset from the shaft axis.

  Embodiment 180-The surgical tool assembly of embodiment 178 or 179, wherein the means for adding further comprises means for selectively locking the surgical end effector in any one of the articulated positions. .

  Example 181- A surgical staple cartridge is configured to be supported within a jaw of a surgical end effector, wherein at least one jaw of the surgical end effector is positioned relative to a second jaw of the surgical end effector. It is movable between an open position and a closed position. The surgical end effector is moved from the unlocked configuration to the locked configuration when the at least one jaw is moved to the closed position to prevent axial movement of the firing member through the surgical end effector. Including a lock member. The surgical end effector includes a cartridge body sized to be seated within the surgical end effector, the cartridge body including a plurality of surgical staples disposed within a staple line and a cam assembly. Operable support. The cam assembly is movable between a start position and an end position within the cartridge body, the cam assembly defining a central axis and a plurality of cam mechanisms thereon, each cam mechanism having a staple line. It corresponds to at least one of them. The cam assembly is laterally offset from the central axis and the cartridge body is seated within the surgical end effector to unlock and engage a corresponding portion of the locking member when the cam assembly is in the starting position. Further comprising: at least one unlocking mechanism on the cam assembly configured to prevent the locking member from reaching the locked configuration when the at least one jaw is moved to the closed position. Prepare.

  Example 182--At least one unlocking mechanism includes a first unlocking ramp formed on a proximal end of a cam assembly at a position laterally offset to one side of a central axis; 182. The surgical staple cartridge of embodiment 181, comprising: a second unlocking ramp formed on the proximal end of the cam assembly at another location laterally offset opposite the axis.

  Example 183. The surgical staple cartridge of Examples 181 or 182, wherein each unlocking mechanism is configured to bias the locking member into an unlocked configuration.

  Example 184- A proximal end of a cam assembly includes a first unlocking ramp configured to be engaged by a firing member as the firing member is advanced axially through the surgical end effector. 182. The surgical staple cartridge of example 182, wherein the cartridge defines a central contact area located between the and the second unlocking ramp.

  Example 185-A surgical end effector comprising a first jaw, an anvil, a firing member, a locking member, and a surgical staple cartridge. The anvil is supported with respect to the first jaw for selectively moving with respect to the first jaw between an open position and a closed position with respect to each other. The firing member is supported to move axially between a start position and an end position within the end effector when the firing and retraction motions are applied. The locking member has a locked configuration in which the firing member is prevented from moving axially through the surgical end effector, and an unlocked configuration in which the firing member is axially advanceable through the surgical end effector. To and from the configured configuration. The surgical staple cartridge includes a cartridge body and a cam assembly. The cartridge body is sized to be seated within the first jaw, and the cartridge body operably supports a plurality of surgical staples disposed therein within a staple line. A cam assembly is movable between a start position and an end position within the cartridge body, the cam assembly defining a central axis and including a plurality of cam mechanisms thereon, each cam mechanism including a staple line. It corresponds to at least one of them. The cam assembly is laterally offset from the central axis and the cartridge body is seated in the first jaw to unlock and engage a corresponding portion of the locking member when the cam assembly is in the starting position. , Further comprising at least one unlocking mechanism on the cam assembly configured to prevent the locking member from reaching the locked configuration when the anvil is moved to the closed position.

  Example 186-At least one unlocking mechanism includes a first unlocking ramp formed on a proximal end of a cam assembly at a location laterally offset to one side of a central axis; 185. The surgical end effector of embodiment 185, wherein the second unlocking ramp is formed on the proximal end of the cam assembly at another location laterally offset opposite the axis.

  Example 187-An anvil is configured to move a locking member in a first direction to lock engagement with a firing member when the anvil is moved to a closed position, wherein each unlocking mechanism includes a corresponding locking member. 189. The surgical end effector of any of embodiments 185 or 186, wherein the surgical end effector is configured to bias the portion to be rotated in a second direction opposite to the first direction.

  Example 188-A proximal end of a cam assembly includes a first unlocking ramp configured to engage with a firing member as the firing member is advanced axially through the surgical end effector. 189. The surgical end effector according to example 186, wherein the end effector defines a central contact area located between the first and second unlocked ramps.

  Example 189-A surgical staple cartridge includes an elongate slot configured to slidably receive a firing member therein when the firing member is moved between a start position and an end position, the locking member comprising: 188. The surgical end effector of any of embodiments 181, 182, 183, or 184, wherein the surgical end effector is configured to axially align the firing member with the elongated slot.

  Example 190-Example 185 wherein the firing member has two sides and the locking member is configured to retainably engage each side of the firing member when the locking member is in the locked configuration. 186, 187, or 188.

  Example 191-A locking member includes a spring arm corresponding to each side of the firing member and a lock notch in each spring arm configured to releasably engage a corresponding locking lug on each side of the firing member. 190. The surgical end effector according to example 190, comprising:

  Example 192. The surgical end effector of any of Examples 185, 186, 187, 188, 190, or 191 wherein the surgical end effector further comprises a tissue cutting surface on the firing member.

  Example 193-An anvil includes an anvil body, an axial slot in the anvil body that allows a portion of the firing member to pass axially therethrough, and each side of the axial slot in the anvil body. 185, 186, 187, 188, 190, 191 or 192, comprising an upper axial passage.

  Example 194-A firing member extends laterally from an upper portion of a firing member body and a foot configured to slidably pass through a corresponding passage in a first jaw and within a body of the anvil. A laterally extending anvil engagement mechanism configured to pass through a corresponding one of the axial passages of the anvil, wherein the first and second engagement mechanisms comprise a foot and an anvil. 193. The surgical end effector according to example 193 positioned between the engagement mechanism.

  Example 195-A surgical staple cartridge is configured to be supported within a jaw of a surgical end effector that defines a shaft axis, wherein at least one jaw of the surgical end effector is a second of the surgical end effector. The jaw is movable between an open position and a closed position. The surgical end effector has a locked configuration in which the firing member is prevented from moving axially through the surgical end effector, and the firing member is axially advanceable through the surgical end effector. A lock member movable between the unlocked configuration and the unlocked configuration. The surgical staple cartridge is a cartridge body sized to be seated in one jaw of a surgical end effector, the cartridge body comprising a plurality of surgical staples disposed therein within a row of staples. Operably supports the cartridge body and staple camming means. And staple cumming means for feeding. The staple cumming means comprises at least one corresponding portion of the locking member laterally offset from the shaft axis when the cartridge body is seated in the jaw of the surgical end effector and the staple cumming means is in the starting position. , Thereby preventing the lock member from reaching the locked configuration when the at least one jaw is moved to the closed position.

  Example 196- A method includes obtaining a first staple cartridge having a first row of staples, and obtaining a second staple cartridge having a second row of staples. And the second row of staples have the same length. The method is to insert a first staple cartridge into a channel having a key-shaped configuration, wherein fully inserting the first staple cartridge into the channel is performed by interference between the key-shaped configuration and the channel. Preventing insertion of the second staple cartridge into the channel, wherein the full insertion of the second staple cartridge into the channel is permitted by the key-shaped configuration; and Further included.

  Example 197-The method of Example 196, wherein inserting the second staple cartridge into the channel further comprises aligning a key feature on the second staple cartridge with a key-type feature on the channel.

  Embodiment 198-The method of embodiment 196 or 197, wherein the method further comprises the bottom surface of the first staple cartridge being spaced from the channel when the first staple cartridge is inserted into the channel.

  Embodiment 199-The method of embodiment 198, wherein the method further comprises that a bottom surface of the second staple cartridge is positioned in contact with the channel when the second staple cartridge is inserted into the channel. .

  Example 200-The method further includes the proximal portion of the first staple cartridge preventing the anvil from clamping against the distal portion of the first staple cartridge when the first staple cartridge is inserted into the channel. 196, 197, 198, or 199.

  Example 201-The method further includes embodiments 196, 197, 198, 199, wherein the firing lockout of the first staple cartridge prevents a firing stroke when the first staple cartridge is inserted into the channel. Or the method of 200.

  Example 202-A method that includes obtaining a first staple cartridge that includes a first amount of staples and obtaining a second staple cartridge that includes a first amount of staples. The method includes inserting the first staple cartridge into a channel having a key-shaped configuration, wherein fully inserting the first staple cartridge into the channel is prevented by the key-shaped configuration. Inserting the first staple cartridge into the channel having a key-shaped configuration, wherein the full insertion of the first staple cartridge into the channel is prevented by the key-shaped configuration. In addition.

  Example 203-The method of example 202, wherein inserting the second staple cartridge into the channel further comprises aligning a key feature on the second staple cartridge with a key-type feature on the channel.

  Embodiment 204- The method of embodiment 202 or 203, wherein the method further comprises wherein a bottom surface of the first staple cartridge is spaced from the channel when the first staple cartridge is inserted into the channel.

  Example 205-The method of example 204, wherein the method further comprises: when the first staple cartridge is inserted into the channel, the bottom surface of the first staple cartridge is spaced from the channel.

  Example 206-The method further comprises the steps 202, 203, 204, wherein the first staple cartridge prevents clamping of the anvil to the first staple cartridge when the first staple cartridge is inserted into the channel. Or 205.

  Embodiment 207-The method further comprises the embodiments 202, 203, 204, 205, wherein the firing lockout of the first staple cartridge prevents a firing stroke when the first staple cartridge is inserted into the channel. Or the method of 206.

  Example 208-The method includes obtaining a channel, obtaining a matching staple cartridge including a proximal alignment protrusion and a distal alignment protrusion, and providing a proximal alignment protrusion with a corresponding proximal Aligning with an alignment mechanism. The method includes: aligning a distal alignment protrusion with a corresponding distal alignment mechanism in a channel; and interlocking the proximal alignment protrusion with a corresponding proximal alignment mechanism to provide distal alignment. Inserting a compatible staple cartridge into the channel such that the protrusion interlocks with the corresponding distal alignment mechanism.

  Example 209-The method of example 208, wherein the method further comprises: when the compatible staple cartridge is inserted into the channel, the bottom surface of the compatible staple cartridge is positioned in contact with the channel.

  Embodiment 210-The method of embodiment 208 or 209, wherein the method further comprises preventing a firing lockout of the conforming staple cartridge from firing stroke until the conforming staple cartridge is inserted into the channel.

  Example 211-The method further comprises attempting to insert a mismatched staple cartridge into the channel, wherein the mismatched staple cartridge further includes an interference mechanism for a corresponding proximal alignment mechanism on the channel. Or the method of 210.

  Example 212-The method of example 211, wherein the method further comprises when a mismatched staple cartridge is inserted into the channel, a bottom surface of the mismatched staple cartridge is spaced from the channel.

  Embodiment 213-The method of embodiment 212, wherein the method further includes the proximal portion of the mismatched staple cartridge preventing the anvil from clamping against the distal portion of the mismatched staple cartridge when the mismatched staple cartridge is inserted into the channel. the method of.

  Embodiment 214-The method of embodiment 211, 212, or 213, wherein the method further comprises preventing the lockout from at least one surgical function when the mismatched staple cartridge is positioned in the channel.

  Example 215-Examples 208, 209, 210, 211, 212 wherein the channel includes a jaw of the end effector and the method further includes matching a classification indicator on the end effector with a classification indicator on the matching staple cartridge. 213, or 214.

  Example 216. A system comprising a replaceable staple cartridge and a channel configured to receive the replaceable staple cartridge. The replaceable staple cartridge includes a plurality of staples, a first downwardly projecting tab, and a second downwardly projecting tab. The channel includes a first container positioned and dimensioned to receive a first downwardly projecting tab, and a second container positioned and dimensioned to receive a second downwardly projecting tab. And a container.

  Example 217-A replaceable staple cartridge further comprises a cartridge body and a pan positioned around a portion of the cartridge body, the pan further comprising a base, a first downwardly projecting tab and a second 218. The system of example 216, wherein the downwardly projecting tab projects from the base.

  Example 218-The system of example 217, wherein the first downwardly protruding tab and the second downwardly protruding tab are comprised of metal.

  Example 219-The exchangeable staple cartridge of any of Examples 216, 217, or 218, further comprising a first laterally extending lug and a second laterally extending lug. system.

  Example 220-A replaceable staple cartridge is a first side wall with a first cutout, wherein the first cutout is positioned and received to receive a first laterally extending lug. A second side wall comprising a first side wall and a second cutout sized, wherein the second cutout is positioned to receive a second laterally extending lug. 229. The system of example 219, further comprising: and sized second sidewalls.

  Example 221-A replaceable staple cartridge further comprises a molded cartridge body, the first laterally extending lugs and the second laterally extending lugs forming the molded cartridge body. 230. The system of example 220, wherein the feature is a configured feature.

  Example 222-The system of example 221, wherein the cartridge body is comprised of a plastic material.

  Example 223- A first laterally extending lug and a second laterally extending lug are located distally of a first downwardly projecting tab and a second downwardly projecting tab. 223. The system of any of embodiments 219, 220, 221 or 222.

  Example 224. A system comprising a replaceable staple cartridge and a channel configured to receive the replaceable staple cartridge. A replaceable staple cartridge includes a plurality of staples and an outer surface including a plurality of ribs. The channel comprises a plurality of slots, each of the slots configured to receive one of the ribs.

  Example 225. The system of example 224, wherein the plurality of ribs include a first rib and a second rib.

  Example 226-The plurality of slots includes a first slot and a second slot, and the channel includes a first sidewall having a first slot, and a second sidewall having a second slot. The system of example 225, further comprising:

  Example 227-The system of any of Examples 224, 225, or 226, wherein the replaceable staple cartridge further comprises a molded cartridge body, and wherein the rib is a molded feature of the molded cartridge body.

  Example 228-The replaceable staple cartridge further comprises an example 224, 225, 226, or 227 further comprising a first laterally extending lug and a second laterally extending lug. The described system.

  Example 229-Channel is a first sidewall with a first cutout, the first cutout being positioned and dimensioned to receive a first laterally extending lug. A second sidewall having a first sidewall and a second cutout, wherein the second cutout is positioned and dimensioned to receive a second laterally extending lug. 224. The system of any of embodiments 224, 225, 226, 227, or 228, further comprising: a second sidewall.

  Example 230-The replaceable staple cartridge further comprises a molded cartridge body, wherein a first laterally extending lug and a second laterally extending lug are disposed within the molded cartridge body. 229. The system of example 229, wherein the system is molded.

  Example 231-The system of Example 230, wherein the molded cartridge body is comprised of a plastic material.

  Example 232-The system of example 231, wherein the first laterally extending lug and the second laterally extending lug are located distally of the rubs.

  Example 233. A system, comprising: a compliant staple cartridge comprising a plurality of staples; and a channel. The system is a means for allowing a conforming staple cartridge to be fully inserted and preventing a mismatched staple cartridge from being fully inserted into a channel, wherein the mismatched staple cartridge and the compatible staple cartridge are of the same length. And means having the same width.

  Example 234. The system of example 233, wherein the means comprises a proximal alignment key and a distal alignment key.

  Example 235. The system of Examples 233 or 234, wherein the system further comprises a second channel, and wherein the mismatched staple cartridge is adapted to the second channel.

  Example 236. A system, comprising: a replaceable staple cartridge; and a channel configured to receive the replaceable staple cartridge. The replaceable staple cartridge includes a plurality of staples, a proximal laterally projecting lug, and a distal laterally projecting lug. The channel includes a proximal container positioned and dimensioned to receive a proximal laterally projecting lug, and a distal container positioned and dimensioned to receive a distal laterally projecting lug. A container.

  Example 237-Example 236 wherein the channel further comprises an obstruction and the replaceable staple cartridge further comprises a complementary anti-obstruction positioned and dimensioned to overcome the obstruction. System.

  Embodiment 238-The system of embodiment 237, wherein the system further comprises a second replaceable staple cartridge with a non-complementary obstacle stop positioned and dimensioned to interfere with the obstacle.

  Example 239-The system of any of Examples 236, 237, or 238, wherein the proximal container defines a cutout in the sidewall and the cutout includes a recess and a protrusion.

  Example 240-The system of example 239, wherein the protrusion is located within the recess.

  Example 241-A second exchange comprising a second plurality of staples, a second proximal laterally projecting lug, and a second distal laterally projecting lug. 240. The system of any of embodiments 236, 237, 238, 239, or 240, further comprising a possible staple cartridge.

  Example 242-A second distal laterally projecting lug is spaced a distance from a second proximal laterally projecting lug, the distance being closer to the replaceable staple cartridge. 241. The system of embodiment 241, wherein the first distance between the laterally projecting lugs and the distal laterally projecting lugs is different.

  Example 243-Second distal laterally projecting lug coincides with distal laterally projecting lug, and second proximal laterally projecting lug projects proximally laterally projecting lug 241. The system of any of embodiments 241 or 242, wherein the lug is different from the lug.

  Example 244-The second replaceable staple cartridge further comprises a deck, the channel further comprises a bottom surface, wherein the deck is moved relative to the bottom surface when the second replaceable staple cartridge is positioned in the channel. 243. The system of any of Examples 241, 242, or 243, wherein the system is obliquely oriented.

  Example 245. The system of example 241, 242, 243, or 244, wherein the replaceable staple cartridge and the second replaceable staple cartridge have the same width and the same length.

  Example 246. The system of example 241, 242, 243, 244, or 245, wherein the plurality of staples and the second plurality of staples comprise the same amount of staples.

  Example 247-Examples 236, 237, 238, 239, 240, 241, 242, 243 wherein distal laterally projecting lugs have a different geometry than proximal laterally projecting lugs. 244, 245, or 246.

  Example 248-The system of example 247, wherein the proximal laterally projecting lugs comprise wedges.

  Example 249-The system of Examples 247 or 248, wherein the proximal laterally projecting lug comprises a cutout that matches a protrusion in the proximal container.

  Example 250-Proximal laterally projecting lugs project from a first side of a replaceable staple cartridge and distal laterally projecting lugs project from a second side of a replaceable staple cartridge , 236, 237, 238, 239, 240, 241, 242, 243, 244, 245, 246, 247, 248, or 249.

  Example 251-an embodiment wherein the replaceable staple cartridge further comprises a deck and the channel further comprises a bottom surface, wherein the deck is parallel to the bottom surface when the replaceable staple cartridge is positioned within the channel. 236, 237, 238, 239, 240, 241, 242, 243, 244, 245, 246, 247, 248, 249, or 250.

  Embodiment 252-A system comprising a channel with an obstruction and a complementary obstruction stop positioned and dimensioned to complement the obstruction when a compatible staple cartridge is received in the channel. A staple cartridge with a non-complementary staple cartridge positioned and dimensioned to interfere with an obstruction when the non-compliant staple cartridge is received in the channel. system.

  Example 253. The system of example 252, wherein the conforming and non-conforming staple cartridges comprise rows of staples of the same length.

  Example 254. The system of Examples 252 or 253, wherein the conforming staple cartridge and the incompatible staple cartridge comprise the same amount of staples.

  Example 255-The system of Examples 252, 253, or 254, wherein the obstacle further comprises a cutout including a recess and a protrusion.

  Example 256-a conforming staple cartridge with a first amount of staples, a non-conforming staple cartridge with a first amount of staples, and a channel that allows full insertion of the conforming staple cartridge, A channel comprising means for preventing full insertion into the channel.

  Example 257-A system, wherein the end effector is configured to receive a compatible replaceable staple cartridge, wherein the end effector comprises a first outer surface, and wherein the classifying identification of the end effector is the second. A compatible replaceable staple cartridge having an end effector, imprinted on one outer surface, having a second outer surface, wherein the classification identification of the compatible replaceable staple cartridge is on the second outer surface. Wherein the classification identification of the compatible replaceable staple cartridge that is engraved on the system corresponds to the classification identification of the end effector.

  Example 258-The system further comprises a non-conforming replaceable staple cartridge, wherein the non-conforming replaceable staple cartridge comprises a third outer surface and the classification identification of the non-conforming replaceable staple cartridge is a third outer staple cartridge. 257. The system of embodiment 257, wherein the classification identification of a compatible replaceable staple cartridge positioned on the surface is different from the classification identification of the end effector.

  Example 259-The system of example 257 or 258, wherein the end effector further comprises a distal portion, and wherein a classification identification of the end effector is positioned on the distal portion.

  Example 260-The system of example 259, wherein the end effector further comprises an anvil, wherein a classification identification of the end effector is positioned at a distal end of the anvil.

  Example 261-Example 257, 258, 259, or 260 wherein the end effector further comprises an anvil comprising a pair of tissue stops, wherein a secondary classification identification of the end effector is positioned over each of the tissue stops. System.

  Example 262-A compatible replaceable staple cartridge further comprises a wedge-shaped distal nose, and the classification identification of the compatible replaceable staple cartridge is on the wedge-shaped distal nose. 257, The system according to example 257, 258, 259, 260, or 261.

  Example 263- The system of any of Examples 257, 258, 259, 260, 261, or 262, wherein the classification label of the end effector and the classification label of the compatible interchangeable staple cartridge include the same alphanumeric characters.

  Example 264. The system of example 263, wherein the same alphanumeric characters indicate the length of the resulting staple line fired from a compatible replaceable staple cartridge.

  Example 265. The system of example 264, wherein the same alphanumeric characters indicate the type of end effector.

  Example 266. The classification identification of the end effector and the classification identification of the compatible replaceable staple cartridge include the same shape, as in Examples 257, 258, 259, 260, 261, 262, 263, 264, or 265. The described system.

  Example 267-Example 257, 258, 259, 260, 261, 262, 263, 263, 264, 265, or the classification identification of the end effector and the classification identification of the compatible replaceable staple cartridge, or 266. The system according to 266.

  Example 268-Examples 257, 258, wherein the system further comprises a lockout configured to prevent at least one surgical function unless a compatible replaceable staple cartridge is positioned within the end effector. 259, 260, 261, 262, 263, 264, 265, 266, or 267.

  Example 269-A system comprising an end effector configured to receive a compatible replaceable staple cartridge, the end effector comprising a first distal end comprising a cartridge compatibility indicator. The system, wherein the compatible replaceable staple cartridge comprises a plurality of staples and the compatible replaceable staple cartridge comprises a second distal end comprising an end effector compatibility indicator.

  Example 270-The system of example 269, wherein the cartridge compatibility indicator is embossed on the outer surface of the end effector.

  Example 271-The system of example 270, wherein the end effector compatibility indicator is embossed on an outer surface of a compatible replaceable staple cartridge.

  Embodiment 272-The cartridge of any of embodiments 269, 270, or 271 wherein the cartridge compatibility indicator longitudinally overlaps the end effector compatibility indicator when a compatible replaceable staple cartridge is positioned within the end effector. system.

  Embodiment 273-A system comprising an end effector configured to receive a compatible replaceable staple cartridge, the end effector comprising a first outer surface comprising a first cord, the end effector comprising: The replaceable staple cartridge comprises a plurality of staples and a second outer surface, wherein the second outer surface comprises a second code, wherein the second code matches the first code.

  Example 274-The system of example 273, wherein the first cord is embossed on the first outer surface and the second cord is embossed on the second outer surface.

  Embodiment 275. The system of embodiment 273 or 274, wherein the first cord and the second cord indicate a compatible replaceable staple cartridge length.

  Example 276. The system of Examples 273, 274, or 275, wherein the first code and the second code include at least one digit and at least one letter.

  Although many of the surgical instrument systems described herein operate with electric motors, the surgical instrument systems described herein can operate in any suitable manner. In various cases, the surgical instrument systems described herein can operate, for example, with a manually operated trigger. In certain examples, the motors disclosed herein may include portions of a robot control system. Further, any of the end effector and / or tool assemblies disclosed herein can be utilized with a robotic surgical instrument system. U.S. Patent Application No. 13 / 118,241, entitled "SURGICAL STAPLING INSTRUMENTS WITH ROTATABLE STAPLE DEPLOYMENT ARRANGEMENTS", and current U.S. Patent Application Publication No. 2012/0298719, for example, describe some examples of robotic surgical instrument systems. Are disclosed in further detail.

  Although the surgical instrument system described herein has been described in connection with staple deployment and deformation, the embodiments described herein are not so limited. Various embodiments are envisioned for deploying fasteners other than staples, such as clamps or tacks. Furthermore, various embodiments are envisioned that utilize any suitable means for sealing tissue. For example, an end effector according to various embodiments may include an electrode configured to heat and seal tissue. Also, for example, an end effector according to certain embodiments can apply vibrational energy to seal tissue.

The entire disclosure below is incorporated herein by reference.
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  Although various instruments have been described herein with particular embodiments, modifications and changes may be made to those embodiments. The particular features, structures, or characteristics may be combined in any suitable manner in one or more embodiments. Thus, a particular feature, structure, or characteristic illustrated or described in connection with one embodiment, without limitation, may be combined in whole or in part with the features, structures, or characteristics of one or more other embodiments. You may. Also, while materials are disclosed with respect to particular components, other materials may be used. Further, according to various embodiments, a single component may be replaced with multiple components to perform a given function (s), and multiple components may be replaced with a single component. It may be replaced. The above description and the following claims are intended to cover all such modifications and variations.

  The devices disclosed herein can be designed to be disposed of after a single use, or they can be designed to be used multiple times. However, in either case, the device may be reconditioned for reuse after at least one use. Reconditioning can include, but is not limited to, any combination of the steps of disassembly of the device, subsequent cleaning or replacement of certain parts of the device, and subsequent reassembly of the device. Specifically, the reconditioning facility and / or surgical team can disassemble the device, clean and / or replace certain parts of the device, and then reassemble the device for future use. Can be. Those skilled in the art will appreciate that reconditioning of a device may utilize various techniques for disassembly, cleaning / replacement, and reassembly. Use of such techniques, and the resulting reconditioned device, are all within the scope of the present application.

  The devices disclosed herein can be processed before surgery. Initially, new or used instruments may be obtained and optionally cleaned. Subsequently, the instrument can be sterilized. In one sterilization technique, the instrument is placed in a closed and sealed container, such as a plastic or TYVEK bag. Subsequently, the container and device can be placed in a radiation field that can penetrate the container, such as gamma rays, X-rays, and / or high energy electrons. Radiation can kill bacteria on instruments and in containers. Subsequently, the sterilized instrument can be stored in a sterile container. The sealed container can keep the instrument sterile until it is opened at the medical facility. The device can also be sterilized using any other technique known in the art, including, but not limited to, beta, gamma, ethylene oxide, hydrogen peroxide plasma, and / or water vapor.

  Although the present invention has been described as having a representative design, the present invention may be further modified within the spirit and scope of the present disclosure. This application is therefore intended to cover any variations, uses, or adaptations of the invention using its general principles.

  All patents, publications, or other disclosures which are hereby incorporated by reference in their entirety or in part, are subject to the existing definitions, descriptions, or other disclosures in which the material incorporated therein is described in this disclosure. It shall be incorporated herein only to the extent not inconsistent with the content. As such, and to the extent necessary, the disclosure as explicitly set forth herein supersedes any conflicting description incorporated herein by reference. Any content that is inconsistent with the current definitions, views, or other disclosures contained herein, or portions thereof, is hereby incorporated by reference, but may be incorporated by reference and the current disclosure. Shall be referenced only to the extent that there is no conflict between

(Embodiment)
(1) a system,
An end effector configured to receive a compatible replaceable staple cartridge, the end effector comprising a first outer surface, wherein a classification identification of the end effector is imprinted on the first outer surface. With an end effector,
The compatible replaceable staple cartridge has a second outer surface, and a classification identification of the compatible replaceable staple cartridge is imprinted on the second outer surface, and the compatible replaceable staple cartridge has a second outer surface. The system wherein the classification identification corresponds to the classification identification of the end effector.
(2) further comprising a non-conforming replaceable staple cartridge, wherein the non-conforming replaceable staple cartridge comprises a third outer surface, wherein the classification identification of the non-conforming replaceable staple cartridge is the third outer surface; The system of claim 1, wherein the classification identification of the matching replaceable staple cartridge positioned thereon is different from the classification identification of the end effector.
The system of claim 1, wherein the end effector further comprises a distal portion, wherein the classification identification of the end effector is positioned on the distal portion.
The system of claim 3, wherein the end effector further comprises an anvil, and wherein the classification identification of the end effector is located at a distal end of the anvil.
The system of claim 1, wherein the end effector further comprises an anvil comprising a pair of tissue stops, wherein a secondary classification identification of the end effector is positioned over each of the tissue stops.

(6) the compatible replaceable staple cartridge further comprises a wedge-shaped distal nose, wherein the classification identification of the compatible replaceable staple cartridge is positioned on the wedge-shaped distal nose. The system of embodiment 1, wherein
7. The system of claim 1, wherein the classification identification of the end effector and the classification identification of the compatible replaceable staple cartridge include the same alphanumeric characters.
The system of claim 7, wherein the same alphanumeric character indicates a length of a resulting staple line fired from the compatible replaceable staple cartridge.
(9) The system according to embodiment 8, wherein the same alphanumeric characters indicate a type of the end effector.
10. The system of claim 1, wherein the classification identification of the end effector and the classification identification of the matching replaceable staple cartridge include the same shape.

The system of claim 1, wherein the classification identification of the end effector and the classification identification of the matching replaceable staple cartridge include the same color.
12. The system of embodiment 1, further comprising a lockout configured to prevent at least one surgical function unless the matching replaceable staple cartridge is positioned within the end effector.
(13) The system,
An end effector configured to receive a compatible replaceable staple cartridge, the end effector comprising a first distal end comprising a cartridge compatibility indicator;
The system wherein the compatible replaceable staple cartridge comprises a plurality of staples and the compatible replaceable staple cartridge comprises a second distal end comprising an end effector compatibility indicator.
The system of claim 13, wherein the cartridge compatibility indicator is embossed on an outer surface of the end effector.
15. The system of claim 14, wherein the end effector compatibility indicator is embossed on an outer surface of the compatible replaceable staple cartridge.

The system of claim 13, wherein the cartridge compatibility indicator longitudinally overlaps the end effector compatibility indicator when the compatible replaceable staple cartridge is positioned within the end effector.
(17) The system,
An end effector configured to receive a compatible replaceable staple cartridge, the end effector comprising a first outer surface comprising a first cord;
The matching replaceable staple cartridge comprises a plurality of staples and a second outer surface, wherein the second outer surface comprises a second cord, wherein the second cord matches the first cord; system.
The system of claim 17, wherein the first cord is embossed on the first outer surface and the second cord is embossed on the second outer surface.
The system of claim 17, wherein the first cord and the second cord indicate a length of the compatible replaceable staple cartridge.
(20) The system of embodiment 17, wherein the first code and the second code include at least one digit and at least one letter.

Claims (20)

System
An end effector configured to receive a compatible replaceable staple cartridge, the end effector comprising a first outer surface, wherein a classification identification of the end effector is imprinted on the first outer surface. With an end effector,
The compatible replaceable staple cartridge has a second outer surface, and a classification identification of the compatible replaceable staple cartridge is imprinted on the second outer surface, and the compatible replaceable staple cartridge has a second outer surface. The system wherein the classification identification corresponds to the classification identification of the end effector.   Further comprising a non-conforming replaceable staple cartridge, wherein the non-conforming replaceable staple cartridge comprises a third outer surface, wherein a classification identification of the non-conforming replaceable staple cartridge is located on the third outer surface. The system of claim 1, wherein the classification identification of the compatible replaceable staple cartridge is different from the classification identification of the end effector.   The system of claim 1, wherein the end effector further comprises a distal portion, wherein the classification identification of the end effector is positioned on the distal portion.   The system of claim 3, wherein the end effector further comprises an anvil, wherein the classification identification of the end effector is located at a distal end of the anvil.   The system of claim 1, wherein the end effector further comprises an anvil comprising a pair of tissue stops, wherein a secondary classification identification of the end effector is positioned over each of the tissue stops.   The compatible replaceable staple cartridge further comprises a wedge-shaped distal nose, wherein the classification identification of the compatible replaceable staple cartridge is positioned on the wedge-shaped distal nose. Item 2. The system according to Item 1.   The system of claim 1, wherein the classification identification of the end effector and the classification identification of the matching replaceable staple cartridge include the same alphanumeric characters.   The system of claim 7, wherein the same alphanumeric character indicates a length of a resulting staple line fired from the compatible replaceable staple cartridge.   9. The system of claim 8, wherein the same alphanumeric characters indicate an end effector type.   The system of claim 1, wherein the classification identification of the end effector and the classification identification of the matching replaceable staple cartridge include the same shape.   The system of claim 1, wherein the classification identification of the end effector and the classification identification of the matching replaceable staple cartridge include the same color.   The system of claim 1, further comprising a lockout configured to prevent at least one surgical function unless the matching replaceable staple cartridge is positioned within the end effector. System
An end effector configured to receive a compatible replaceable staple cartridge, the end effector comprising a first distal end comprising a cartridge compatibility indicator;
The system wherein the compatible replaceable staple cartridge comprises a plurality of staples and the compatible replaceable staple cartridge comprises a second distal end comprising an end effector compatibility indicator.   14. The system of claim 13, wherein the cartridge compatibility indicator is embossed on an outer surface of the end effector.   15. The system of claim 14, wherein the end effector compatibility indicator is embossed on an outer surface of the compatible replaceable staple cartridge.   14. The system of claim 13, wherein the cartridge compatibility indicator longitudinally overlaps the end effector compatibility indicator when the compatible replaceable staple cartridge is positioned within the end effector. System
An end effector configured to receive a compatible replaceable staple cartridge, the end effector comprising a first outer surface comprising a first cord;
The matching replaceable staple cartridge comprises a plurality of staples and a second outer surface, wherein the second outer surface comprises a second cord, wherein the second cord matches the first cord; system.   20. The system of claim 17, wherein the first cord is embossed on the first outer surface and the second cord is embossed on the second outer surface.   20. The system of claim 17, wherein the first code and the second code indicate a length of the compatible replaceable staple cartridge.   The system of claim 17, wherein the first code and the second code include at least one digit and at least one letter.

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