CA2851239A1 - Electrical surgical instrument - Google Patents

Abstract

A surgical instrument includes a surgical end effector having a receiving portion for removably receiving therein an interchangeable part. The receiving portion has a communication connection. A handle connected to the end effector actuates the end effector. The handle has a controller electrically connected to the communication connection for authenticating the interchangeable part when placed at the end effector. An interchangeable part is removably connected to the receiving portion and has an encryption device electrically removably connected to the communication connection when placed at the receiving portion. The encryption device authenticates the interchangeable part when queried by the electric controller.

Description

ELECTRICAL SURGICAL INSTRUMENT
This application is a divisional of Canadian patent application Serial No.

2,715,183, which in turn is a divisional of Canadian Patent application Serial No. 2,619,276 tiled internationally on May 31, 2007 and entered nationally on May 8,2008.
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Technical Field The present invention lies in the field of surgical instruments, in particular but not necessarily, stapling devices. The stapling device described in the present application is a hand-held, fully electrically powered and controlled surgical stapler.
Medical stapling devices exist in the art. Ethicon Endo-Surgery, Inc. (a Johnson &
Johnson company; hereinafter "Ethicon") manufactures and sells such stapling devices. Circular stapling devices manufactured by Ethicon are referred to under the trade names PROXIMATE
PPH, CDH, and ILS and linear staplers are manufactured by Ethicon under the trade names CONTOUR and PROXIMATE. In each of these exemplary surgical staplers, tissue is compressed between a staple cartridge and an anvil and, when the staples are ejected, the compressed tissue is also cut. Depending upon the particular tissue engaged by the physician, the tissue can be compressed too little (where blood color is still visibly present in the tissue),,too much (where tissue is crushed), or correctly (where the liquid is removed from the tissue, referred to as dessicating or blanching).
Staples to be delivered have a given length and the cartridge and anvil need to be within an acceptable staple firing distance so that the staples close properly upon firing. Therefore, these staplers have devices indicating the relative distance between the two planes and whether or not this distance is within the staple length firing range. Such an indicator is mechanical and takes the form of a sliding bar behind a window having indicated thereon a safe staple-firing range. These staplers are all hand-powered, in other words, they require physical actuations by the user/physician to position the anvil and stapler cartridge about the tissue to be stapled and/or cut, to close the anvil and stapler cartridge with respect to one another, and to fire and secure the staples at the tissue (and/or cut the tissue). No prior art staplers are electrically powered to carry out each of these operations because the longitudinal force necessary to effect staple firing is typically on the order of 250 pounds at the staple cartridge. Further, such staplers do not have any kind of active compression indicator that would optimizes the force acting upon the tissue that is to be stapled so that tissue degradation does not occur.

One hand-powered, intraluminal anastomotic circular stapler is depicted in, for example, in U.S.
Patent No. 5,104,025 to Main etal., and assigned to Ethicon. As can be seen most clearly in the exploded view of FIG. 7 in Main et al., a trocar shaft 22 has a distal indentation 21, some recesses 28 for aligning the trocar shaft 22 to serrations 29 in the anvil and, thereby, align the staples with the anvils 34. A
trocar tip 26 is capable of puncturing through tissue when pressure is applied thereto. FIGS. 3 to 6 in Main et al. show how the circular stapler 10 functions to join two pieces of tissue together. As the anvil 30 is moved closer to the head 20, interposed tissue is compressed therebetwoen, as particularly shown in FIGS. 5 and 6. If this tissue is overcompressed, the surgical stapling procedure might not succeed. Thus, it is desirable to not exceed the maximum acceptable tissue compression force. The interposed tissue can be subject to a range of acceptable compressing force during surgery. This range is known and refi..LITII to as optimal tissue compression or OTC, and is dependent upon the type of tissue being stapled. While the stapler shown in Main etal.
does have a bar indicator that displays to the user a safe staple-firing distance between the anvil and the staple cartridge, it cannot indicate to the user any level of compressive force being imparted upon the tissue prior to stapling. It would be desirable to provide such an indication so that over-compression of the tissue can be avoided.
Disclosure of Invention The invention overcomes the above-noted and other deficiencies of the prior art by providing an electric surgical stapling device that is electrically powered to position the anvil and stapler cartridge with respect to one another about the tissue to be stapled and/or cut, to close the anvil and stapler cartridge with respect to one another, and to fire and secure the staples at the tissue (and/or cut the tissue). Further, the electric surgical stapling device can indicate to the user a user-pre-defmed level of compressive force being imparted upon the tissue prior to firing the staples. The present invention also provides methods for operating the electric surgical stapling device to staple when OTC exists.
An offset-axis configuration for the two anvil and staple firing sub-assemblies creates a device that can be sized to comfortably fit into a user's hand. It also decreases manufacturing difficulty by removing previously required nested (co-axial) hollow shafts.
With the axis of the anvil sub-assembly being offset from the staple firing sub-assembly, the length of the threaded rod

3 for extending and retracting the anvil can be decreased by approximately two inches, thereby saving in manufacturing cost and generating a shorter longitudinal profile.
An exemplary method for using the electric stapler includes a power-on feature that permits entry into a manual mode for testing purposes. In a surgical procedure, the stapler is a one-way device. In the test mode, however, the user has the ability to move the trocar back and forth as desired. This test mode can be disengaged and the stapler reset to the use mode for packaging and shipment_ For packaging, it is desirable (but not necessary) to have the anvil be at a distance from the staple cartridge. Therefore, a homing sequence can be programmed to place the anvil 1 cm (for example) away from the staple cartridge before powering down for packaging and shipment. Before use, the trocar is extended and the anvil is removed. If the stapler is being used to dissect a colon, for example, the trocar is retracted back into the handle and the handle is inserted trans-anally into the colon to downstream side of the dissection while the anvil is inserted through a laparoscopic incision to an upstream side of the dissection. The anvil is attached to the trocar and the two parts are retracted towards the handle until a staple ready condition occurs. The staple firing sequence is started, which can be aborted, to staple the dissection and simultaneously cut tissue at the center of the dissection to clear an opening in the middle of the circular ring of staples. The staple firing sequence includes an optimal tissue compression (OTC) measurement and feedback control mechanism that causes staples to be fired only when the compression is in a desired pressure range, referred to as the OTC range. This range or value is known beforehand based upon known characteristics of the tissue to be compressed between the anvil and staple cartridge.
Some exemplary procedures in which the electric stapler can be used include colon dissection and gastric bypass surgeries. There are many other uses for the electric stapler in various different technology areas.
With the objects of the invention in view, there is also provided a surgical instrument, including a surgical end effector having at least one actuation assembly to effect a surgical procedure when actuated, an electric motor operationally connected to the end effector to operate the at least one actuation assembly, and a power supply electrically connected to the motor and selectively powering the motor to actuate the at least one actuation assembly.
The power supply has at least one battery cell with a critical current rate. When activated to power the motor and

4 actuate the at least one actuation assembly, the power supply operates the at least one battery cell at a super-critical current rate.
With the objects of the invention in view, there is also provided a surgical instrument, including a surgical end effector having at least one actuation assembly to effect a surgical procedure when actuated, an electric motor operationally connected to the end effector to operate the at least one actuation assembly, and a power supply electrically connected to the motor and selectively powering the motor to actuate the at least one actuation assembly.
The power supply has at least one battery cell with a critical current rate, and, when activated to power the motor and actuate the at least one actuation assembly, the power supply operates the at least one battery cell at an average current rate above the critical current rate.
With the objects of the invention in view, there is also provided a surgical instrument, including a surgical end effector having at least one actuation assembly to effect a surgical procedure when actuated, an electric motor operationally connected to the end effector to operate the at least one actuation assembly, and a power supply electrically connected to the motor and selectively powering the motor to actuate the at least one actuation assembly at least 1 and less than 16 times during a clinical life of at least one of the end effector, the motor, and the power supply. The power supply has at least one battery cell that, when activated to actuate the at least one actuation assembly, operates only between approximately 0.5 seconds and approximately 15 seconds in duration.
With the objects of the invention in view, there is also provided a surgical instrument, including a surgical end effector having at least one actuation assembly to effect a surgical procedure when actuated, an electric motor having a rated operating voltage and being operationally connected to the end effector to operate the at least one actuation assembly, and a power supply electrically connected to the motor and selectively powering the motor to actuate the at least one actuation assembly. The power supply has at least one battery cell with a critical current rate. When activated to power the motor and actuate the at least one actuation assembly, the power supply operates the at least one battery cell at a super-critical current rate at any time during at least a portion of a super-critical pulse discharge period and operates the motor above the rated operating voltage during the super-critical pulse discharge period.
Other features that are considered as characteristic for the invention are set forth in the appended claims.

Although the invention is illustrated and described herein as embodied in an electrical surgical instrument with optimized power supply and drive, it is, nevertheless, not intended to be limited to the details shown because various modifications and structural changes may be made

5 therein without departing from the spirit of the invention and within the scope and range of equivalents of the claims.
The construction and method of operation of the invention, however, together with additional objects and advantages thereof, will be best understood from the following description of specific embodiments when read in connection with the accompanying drawings.
Brief Description of Drawings Advantages of embodiments of the present invention will be apparent from the following detailed description of the preferred embodiments thereof, which description should be considered in conjunction with the accompanying drawings in which:
FIG. 1 is a perspective view from a side of an exemplary embodiment of an electric stapler according to the invention;
FIG. 2 is a fragmentary side elevational view of the stapler of FIG. 1 with a right half of a handle body and with a proximal backbone plate removed;
FIG. 3 is an exploded, perspective view of an anvil control assembly of the stapler of FIG.
1;
FIG. 4 is an enlarged, fragmentary, exploded, perspective view of the anvil control assembly of FIG. 3;
FIG. 5 is a fragmentary, perspective view of a staple firing control assembly of the stapler of FIG. 1 from a rear side thereof, FIG. 6 is an exploded, perspective view of the staple firing control assembly of the stapler of FIG, 1;
FIG. 7 is an enlarged, fragmentary, exploded, perspective view of the staple firing control assembly of FIG. 6;
FIG. 8 is a fragmentary, horizontally cross-sectional view of the anvil control assembly from below the handle body portion of the stapler of FIG. 1;
FIG. 9 is a fragmentary, enlarged, horizontally cross-sectional view from below a proximal portion of the anvil control assembly FIG. 8;

6 FIG. 10 is a fragmentary, enlarged, horizontally cross-sectional view from below an intermediate portion of the anvil control assembly of FIG. 8;
FIG. 11 is a fragmentary, enlarged, horizontally cross-sectional view from below a distal portion of the anvil control assembly of FIG. 8;
FIG. 12 is a fragmentary, vertically cross-sectional view from a right side of a handle body portion of the stapler of FIG. 1;
FIG. 13 is a fragmentary, enlarged, vertically cross-sectional view from the right side of a proximal handle body portion of the stapler of FIG. 12;
FIG. 14 is a fragmentary, enlarged, vertically cross-sectional view from the right side of an intermediate handle body portion of the stapler of FIG. 12;
FIG. 15 is a fragmentary, further enlarged, vertically cross-sectional view from the right side of the intermediate handle body portion of the stapler of FIG. 14;
FIG. 16 is a fragmentary, enlarged, vertically cross-sectional view from the right side of a distal handle body portion of the stapler of FIG. 12;
FIG. 17 is a perspective view of a portion of an anvil of the stapler of FIG.
1;
FIG. 18 is a fragmentary, cross-sectional view of a removable stapling assembly including the anvil, a stapler cartridge, a force switch, and a removable cartridge connecting assembly of the stapler of FIG. 1;
FIG. 19 is a fragmentary, horizontally cross-sectional view of the anvil control assembly from above the handle body portion of the stapler of FIG. 1 with the anvil rod in a fully extended position;
FIG. 20 is a fragmentary, side elevational view of the handle body portion of the stapler of FIG. 1 from a left side of the handle body portion with the left handle body and the circuit board removed and with the anvil rod in a fully extended position;
FIG. 21 is a fragmentary, side elevational view of the handle body portion of the stapler of FIG. 20 with the anvil rod in a 1-cm anvil closure position;
FIG. 22 is a fragmentary, horizontally cross-sectional view of the anvil control assembly from above the handle body portion of the stapler of FIG. 1 with the anvil rod in a safe staple firing position;

7 FIG. 23 is a fragmentary, horizontally cross-sectional view of the anvil control assembly from above the handle body portion of the stapler of FIG. 1 with the anvil rod in a fully retracted position;
FIG. 24 is a fragmentary, horizontally cross-sectional view of the firing control assembly from above the handle body portion of the stapler of FIG. 1;
FIG. 25 is a fragmentary, enlarged, horizontally cross-sectional view from above a proximal portion of the firing control assembly of FIG. 24;
FIG. 26 is a fragmentary, enlarged, horizontally cross-sectional view from above an intermediate portion of the firing control assembly of FIG. 24;
FIG. 27 is a fragmentary, enlarged, horizontally cross-sectional view from above a distal portion of the firing control assembly of FIG. 24;
FIGS. 28 and 29 are shaded, fragmentary, enlarged, partially transparent perspective views of a staple cartridge removal assembly of the stapler of FIG. 1;
FIG. 30 is a schematic circuit diagram of an exemplary encryption circuit for interchangeable parts of the medical device according to the invention;
FIG. 31 is a bar graph illustrating a speed that a pinion moves a rack shown in FIG. 32 for various loads;
FIG. 32 is a fragmentary, perspective view of a simplified, exemplary portion of a gear train according to the present invention between a gear box and a rack;
FIG. 33 is a fragmentary, vertically longitudinal, cross-sectional view of a distal end of an articulating portion of an exemplary embodiment of an end effector with the inner tube, the pushrod-blade support, the anvil, the closure ring, and the near half of the staple sled removed;
FIG. 34 is a schematic circuit diagram of an exemplary switching assembly for a power supply according to the invention;
FIG. 35 is a schematic circuit diagram of an exemplary switching assembly for forward and reverse control of a motor according to the invention; and FIG. 36 is a schematic circuit diagram of another exemplary switching assembly for the power supply and the forward and reverse control of the motor according to the invention.

8 Best Mode for Carryine Out the Invention Aspects of the invention are disclosed in the following description and related drawings directed to specific embodiments of the invention. Alternate embodiments may be devised without departing from the spirit or the scope of the invention. Additionally, well-known elements of exemplary embodiments of the invention will not be described in detail or will be omitted so as not to obscure the relevant details of the invention.
Before the present invention is disclosed and described, it is to be understood that the terminology used herein is for the purpose of describing particular embodiments only and is not intended to be limiting. It must be noted that, as used in the specification and the appended claims, the singular forms "a," "an," and "the" include plural references unless the context clearly dictates otherwise.
While the specification concludes with claims defining the features of the invention that are regarded as novel, it is believed that the invention will be better understood from a consideration of the following description in conjunction with the drawing figures, in which like reference numerals are carried forward. The figures of the drawings are not drawn to scale.
Further, it is noted that the figures have been created using a computer-aided design computer program. This program at times removes certain structural lines and/or surfaces when switching from a shaded or colored view to a wireframe view. Accordingly, the drawings should be treated as approximations and be used as illustrative of the features of the present invention.
Referring now to the figures of the drawings in detail and first, particularly to FIGS. 1 to 2 thereof, there is shown an exemplary embodiment of an electric surgical circular stapler 1. The present application applies the electrically powered handle to a circular surgical staple head for ease of understanding only. The invention is not limited to circular staplers and can be applied to any surgical stapling head, such as a linear stapling device, for example.
The powered stapler 1 has a handle body 10 containing three switches: an anvil open switch 20, an anvil close switch 21, and a staple firing switch 22. Each of these switches is electrically connected to a circuit board 500 (see FIG. 12) having circuitry programmed to carry out the stapling functions of the stapler 1. The circuit board 500 is electrically connected to a power supply 600 contained within the handle body 10. One exemplary embodiment utilizes 2 to 6 Lithium CR123 or CR2 cells as the power supply 600. Other power supply embodiments are possible, such as rechargeable batteries or a power converter that is connected to an electric mains

9 (in the latter embodiment, the stapler would not be self-powered or self-contained). As used herein, the terms self-powered or self-contained when used with regard to the electric power supply (600) are interchangeable and mean that the power supply is a complete and independent unit in and of itself and can operate under its own power without the use of external power sources. For example, a power supply having an electric cord that is plugged into an electric mains during use is not self-powered or self-contained.
Insulated conductive wires or conductor tracks on the circuit board SOO
connect all of the electronic parts of the stapler 1, such as an on/off switch 12, a tissue compression indicator 14, the anvil and firing switches 20, 21, 22, the circuit board 500, and the power supply 600, for example.
But these wires and conductors are not shown in the figures of the drawings for ease of understanding and clarity.
The distal end of the handle body 10 is connected to a proximal end of a rigid anvil neck 30. Opposite this connection, at the distal end of the anvil neck 30, is a coupling device 40 for removably attaching a staple cartridge 50 and an anvil 60 thereto.
Alternatively, the staple cartridge 50 can be non-removable in a single-use configuration of the stapler 1. These connections will be described in further detail below.
FIG. 2 shows the handle body 10 with the right half 13 of the handle body 10 and the circuit board 500 removed. As will be discussed below, a proximal backbone plate 70 is also removed from the view of FIG. 2 to allow viewing of the internal components inside the handle body 10 from the right side thereof. What can be seen from the view of FIG. 2 is that there exist two internal component axes within the handle body 10. A first of these axes is the staple control axis 80, which is relatively horizontal in the view of FIG. 2. The staple control axis 80 is the centerline on which lie the components for controlling staple actuation. The second of these axes is the anvil control axis 90 and is disposed at an angle to the staple control axis 80. The anvil control axis 90 is the centerline on which lie the components for controlling anvil actuation. It is this separation of axes 80, 90 that allows the electric stapler 1 to be powered using a handle body

10 that is small enough to fit in a physician's hand and that does not take up so much space that the physician becomes restricted from movement in all necessary directions and orientations.
Shown inside the handle body 10 is the on/off switch 12 (e.g., a grenade pin) for controlling power (e.g., battery power) to all of the electrical components and the tissue compression indicator 14. The tissue compression indicator 14 indicates to the physician that the tissue being compressed between the anvil 60 and the staple cartridge 50 has or has not been compressed with greater than a pre-set compressive force, which will be described in further detail below. This indicator 14 is associated with a force switch 400 that has been described in co -5 pending U.S. Patent Provisional Application Serial No. 60/801,989 filed May 19, 2006, and titled "Force Switch" (the entirety of which is incorporated by reference herein).
The components along the anvil control axis 90 make up the anvil control assembly 100.
An anvil control frame 110 is aligned along the anvil control axis 90 to house and/or fix various part of the anvil control assembly 100 thereto. The anvil control frame 110 has a proximal mount 10 112, an intermediate mount 114, and a distal mount 116. Each of these mounts 112, 114, 116 can be attached to or integral with the control frame 110. In the exemplary embodiment, for ease of manufacturing, the proximal mount 112 has two halves and is separate from the frame 110 and the intermediate mount 114 is separate from the frame 110.
At the proximal end of the anvil control assembly 100 is an anvil motor 120.
The anvil motor 120 includes the drive motor and any gearbox that would be needed to convert the native motor revolution speed to a desired output axle revolution speed. In the present case, the drive motor has a native speed of approximately 10,000 rpm and the gearbox converts the speed down to between approximately 50 and 70 rpm at an axle 122 extending out from a distal end of the anvil motor 120. The anvil motor 120 is secured both longitudinally and rotationally inside the proximal mount 112.
A motor-shall coupler 130 is rotationally fixed to the axle 122 so that rotation of the axle 122 translates into a corresponding rotation of the motor coupler 130.
Positioned distal of the coupler 130 is a rotating nut assembly 140. The nut assembly 140 is, in this embodiment, a two part device having a proximal nut half 141 and a distal nut half 142 rotationally and longitudinally fixed to the proximal nut half 141. It is noted that these nut halves 141, 142 can be integral if desired. Here, they are illustrated in two halves for ease of manufacturing. The proximal end of the nut assembly 140 is rotationally fixed to the distal end of the coupler 130. Longitudinal and rotational support throughout the length of these two connected parts is assisted by the intermediate 114 and distal 116 mounts.
A proximal nut bushing 150 (see FIG. 3) is interposed between the intermediate mount 114 and the proximal nut half 141 and a distal nut bushing 160 is interposed between the distal mount 116 and the distal nut half 142 to have these parts spin efficiently and substantially without friction

11 within the handle body 10 and the anvil control frame 110. The bushings 150, 160 can be of any suitable bearing material, for example, they can be of metal such as bronze or a polymer such as nylon. To further decrease the longitudinal friction between the rotating nut assembly 140 and the coupler 130, a thrust washer 170 is disposed between the proximal bushing 150 and the proximal nut half 141.
Rotation of the coupler 130 and nut assembly 140 is used to advance or retract a threaded rod 180, which is the mechanism through which the anvil 60 is extended or retracted. The threaded rod 180 is shown in further detail in the exploded view of FIGS. 3 to 4 and is described in further detail below. A rod support 190 is attached to a distal end of the anvil control frame 110 for extending the supporting surfaces inside the nut assembly 140 that keep the rod 180 aligned along the anvil control axis 90. The rod support 190 has a smooth interior shape corresponding to an external shape of the portion of the rod 180 that passes therethrough. This mating of shapes allows the rod 180 to move proximally and distally through the support 190 substantially without friction. To improve frictionless movement of the rod 180 through the support 190, in the exemplary embodiment, a cylindrical rod bushing 192 is disposed between the support 190 and the rod 180. The rod bushing 192 is not visible in FIG. 2 because it rests inside the support 190.
However, the rod bushing 192 is visible in the exploded view of FIGS. 3 to 4.
With the rod bushing 192 in place, the internal shape of the support 190 corresponds to the external shape of the rod bushing 192 and the internal shape of the rod bushing 192 corresponds to the external shape of the portion of the rod 180 that passes therethrough. The rod bushing 192 can be, for example, of metal such as bronze or a polymer such as nylon.
The components along the staple control axis 80 form the staple control assembly 200.
The staple control assembly 200 is illustrated in FIG. 5 viewed from a proximal upper and side perspective. The proximal end of the staple control assembly 200 includes a stapling motor 210.
The stapling motor 210 includes the drive motor and any gearbox that would be needed to convert the native motor revolution speed to a desired revolution speed. In the present case, the drive motor has a native speed of approximately 20,000 rpm and the gearbox converts the speed to approximately 200 rpm at an output axle 212 at the distal end of the gearbox.
The axle 212 cannot be seen in the view of FIG. 5 but can be seen in the exploded view of FIGS. 6 to 7.
The stapling motor 210 is rotationally and longitudinally fixed to a motor mount 220.
Distal of the motor mount 220 is an intermediate coupling mount 230. This coupling mount 230

12 has a distal plate 232 that is shown, for example in FIG. 6. The distal plate 232 is removable from the coupling mount 230 so that a rotating screw 250 can be held therebetween.
It is this rotating screw 250 that acts as the drive for ejecting the staples out of the staple cartridge 50. The efficiency in transferring the rotational movement of axle 212 to the rotating screw 250 is a factor that can substantially decrease the ability of the stapler 1 to deliver the necessary staple ejection longitudinal force of up to 250 pounds. Thus, an exemplary embodiment of the screw 250 has an acme profile thread.
There are two exemplary ways described herein for efficiently coupling the rotation of the axle 212 to the screw 250. First, the stapling motor 210 can be housed "loosely" within a chamber defined by the handle body 10 so that it is rotationally stable but has play to move radially and so that it is longitudinally stable but has play to move. In such a configuration, the stapling motor 210 will "find its own center" to align the axis of the axle 212 to the axis of the screw 250, which, in the exemplary embodiment, is also the staple control axis 80.
A second exemplary embodiment for aligning the axle 212 and the screw 250 is illustrated in FIGS. 1 to 5, for example. In this embodiment, a proximal end of a flexible coupling 240 is fixed (both rotationally and longitudinally) to the axle 212. This connection is formed by fitting the distal end of the axle 212 inside a proximal bore 241 of the flexible coupling 240. Sec FIG.
12. The axle 212 is, then, secured therein with a proximal setscrew 213. The screw 250 has a proximal extension 251 that fits inside a distal bore 242 of the flexible coupling 240 and is secured therein by a distal setscrew 252. It is noted that the figures of the drawings show the flexible coupling 240 with ridges in the middle portion thereof In an exemplary embodiment of the coupling 240, the part is of aluminum or molded plastic and has a spiral or helixed cut-out around the circumference of the center portion thereof. In such a configuration, one end of the coupling 240 can move in any radial direction (360 degrees) with respect to the other end (as in a gimbal), thus providing the desired flex to efficiently align the central axes of the axle 212 and the screw 250.
The proximal extension 251 of the screw 250 is substantially smaller in diameter than the diameter of the bore 231 that exists in and through the intermediate coupling mount 230. This bore 231 has two increasing steps in diameter on the distal side thereof. The first increasing step in diameter is sized to fit a proximal radius screw bushing 260, which is formed of a material that is softer than the intermediate coupling mount 230. The proximal radius screw bushing 260 only

13 keeps the screw 250 axially aligned and does not absorb or transmit any of the longitudinal thrust.
The second increasing step in diameter is sized to fit a proximal thrust bearing 270 for the screw 250. In an exemplary embodiment of the thrust bearing 270, proximal and distal plates sandwich a bearing ball retainer plate and bearing balls therebetween. This thrust bearing 270 absorbs all of the longitudinal thrust that is imparted towards the axle 212 while the up to 250 pounds of longitudinal force is being applied to eject the staples in the staple cartridge 50. The proximal extension 251 of the screw 250 has different sized diameters for each of the interiors of the screw bushing 260 and the thrust bearing 270. The motor mount 220 and the coupling mount 230, therefore, form the two devices that hold the flexible coupling 240 therebetween.
The rotating screw 250 is held inside the distal plate 232 with a distal radius screw bushing 280 similar to the proximal radius screw bushing 260. Thus, the screw 250 rotates freely within the distal plate 232. To translate the rotation of the screw 250 into a linear distal movement, the screw 250 is threaded within a moving nut 290. Movement of the nut 290 is limited to the amount of movement that is needed for complete actuation of the staples; in other words, the nut 290 only needs to move through a distance sufficient to form closed staples between the staple cartridge 50 and the anvil 60 and to extend the cutting blade, if any, within the staple cartridge 50, and then retract the same. When the nut 290 is in the proximal-most position (see, e.g., FIG. 12), the staples are at rest and ready to be fired. When the nut 290 is in the distal-most position, the staples are stapled through and around the tissue interposed between the staple cartridge 50 and the anvil, and the knife, if any, is passed entirely through the tissue to be cut. The distal-most position of the nut 290 is limited by the location of the distal plate 232. Thus, the longitudinal length of the threads of the screw 250 and the location of the distal plate 232 limit the distal movement of the nut 290.
Frictional losses between the screw 250 and the nut 290 contribute to a significant reduction in the total pounds of force that can be transmitted to the staple cartridge 50 through the cartridge plunger 320. Therefore, it is desirable to select the materials of the screw 250 and the nut 290 and the pitch of the threads of the screw 250 in an optimized way. It has been found that use of a low-friction polymer for manufacturing the nut 290 will decrease the friction enough to transmit the approximately 250 pounds of longitudinal force to the distal end of the cartridge plunger 320 ¨ the amount of force that is needed to effectively deploy the staples. Two particular exemplary materials provide the desired characteristics and are referred to in the art as DELRIN

14 AF Blend Acetal (a thermoplastic material combining TEFLON fibers uniformly dispersed in DELRINO acetal resin) and RULON (a compounded form of TEE fluorocarbon) or other similar low-friction polymers.
A nut coupling bracket 300 is longitudinally fixed to the nut 290 so that it moves along with the nut 290. The nut coupling bracket 300 provides support for the relatively soft, lubricious nut material. In the exemplary embodiment shown, the bracket 300 has an interior cavity having a shape corresponding to the exterior shape of the nut 290. Thus, the nut 290 fits snugly into the coupling bracket 300 and movement of the nut 290 translates into a corresponding movement of the nut coupling bracket 300. The shape of the nut coupling bracket 300 is, in the exemplary embodiment, dictated by the components surrounding it and by the longitudinal forces that it has to bear. For example, there is an interior cavity 302 distal of the nut 290 that is shaped to receive the distal plate 232 therein. The nut coupling bracket 300 also has a distal housing 304 for receiving therein a stiffening rod 310. The stiffening rod 310 increases the longitudin4 support and forms a portion of the connection between the nut 290 and a cartridge plunger 320 (see, i.e., FIG. 5), which is the last moving link between elements in the handle body 10 and the staple cartridge 50. A firing bracket 330, disposed between the distal end of the nut coupling bracket 300 and the stiffening rod 310, strengthens the connection between the nut coupling bracket 300 and the rod 310.
Various components of the stapler 1 are connected to one another to form a backbone or spine. This backbone is a frame providing multi-directional stability and is made up of four primary parts (in order from proximal to distal): the anvil control frame 110, the proximal backbone plate 70 (shown in FIGS. 3 to 4 and 610 7), a distal backbone plate 340, and the anvil neck 30. Each of these four parts is longitudinally and rotationally fixed to one another in this order and forms the skeleton on which the remainder of the handle components is attached in some way. Lateral support to the components is provided by contours on the inside surfaces of the handle body 10, which in an exemplary embodiment is formed of two halves, a left half 11 and a right half 13. Alternatively, support could be single frame, stamped, or incorporated into the handle halves 11, 13.
Functionality of the anvil control assembly 100 is described with regard to FIGS. 17 to 27.
To carry out a stapling procedure with the stapler 1, the anvil 60 is removed entirely from the stapler 1 as shown in FIG. 17. The anvil open switch 20 is depressed to extend the distal end of the trocar tip 410 housed within the staple cartridge and which is longitudinally fixedly connected to the screw 250. The point of the trocar tip 410 can, now, be passed through or punctured through tissue that is to be stapled. The user can, at this point, replace the anvil 60 onto the trocar 5 tip 410 from the opposite side of the tissue (see FIG. 18) and, thereby, lock the anvil 60 thereon.
The anvil closed switch 22 can be actuated to begin closing the anvil 60 against the staple cartridge 50 and pinch the tissue therebetween within an anvil-cartridge gap 62.
To describe how the trocar tip controlling movement of the anvil 60 occurs, reference is made to FIGS. 8 to 10, 14 to 15, and 18. As shown in dashed lines in FIG. 15, a rod-guiding pin 10 143 is positioned within the central bore 144 of the distal nut half 142. As the threaded rod 180 is screwed into the rotating nut 140, 141, 142, the pin 143 catches the proximal end of the thread 182 to surround the pin 143 therein. Thus, rotation of the nut 140 with the pin 143 inside the thread 182 will cause proximal or distal movement of the rod 180, depending on the direction of nut rotation. The thread 182 has a variable pitch, as shown in FIGS. 14 to 15, to move the anvil 60 at

15 different longitudinal speeds. When the pin 143 is inside the longer (lower) pitched thread portion 183, the anvil 60 moves longitudinally faster. In comparison, when the pin 143 is inside the shorter (higher) pitched thread portion 184, the anvil 60 moves longitudinally slower. It is noted that the pin 143 is the only portion contacting the thread 182 when in the longer pitched thread portion 183. Thus, the pin 143 is exposed to the entire longitudinal force that is acting on the rod 180 at this point in time. The pin 143 is strong enough to bear such forces but may not be sufficient to withstand all longitudinal force that could occur with anvil 60 closure about interposed tissue.
As shown in FIG. 14, the rod 180 is provided with a shorter pitched thread portion 184 to engage in a corresponding internal thread 145 at the proximal end of the central bore 144 of the proximal nut half 141. When the shorter pitched thread portion 184 engages the internal thread 145, the entire transverse surface of the thread portion 184 contacts the internal thread 145. This surface contact is much larger than the contact between the pin 143 and any portion of the thread 182 and, therefore, can withstand all the longitudinal force that occurs with respect to anvil 60 closure, especially when the anvil 60 is closing about tissue during the staple firing state. For example, in the exemplary embodiment, the pin 143 bears up to approximately 30 to 50 pounds of longitudinal force. This is compared to the threads, which can hold up to 400 pounds of longitudinal force ¨ an almost 10-to-1 difference.

16 An alternative exemplary embodiment of anvil control assembly 100 can entirely remove the complex threading of the rod 180. In such a case, the rod 180 has a single thread pitch and the anvil motor 120 is driven (through corresponding programming in the circuit board 500) at different speeds dependent upon the longitudinal position of the single-thread rod 180.
In any embodiment for driving the motors 120, 210, the control programming can take many forms. In one exemplary embodiment, the microcontroller on the battery powered circuit board 500 can apply pulse modulation (e.g., pulse-width, pulse-frequency) to drive either or both of the motors. Further, because the stapler 1 is a device that has a low duty cycle, or is a one-use device, components can be driven to exceed acceptable manufacturers' specifications. For example, a gear box can be torqued beyond its specified rating. Also, a drive motor, for example, a 6 volt motor, can be overpowered, for example, with 12 volts.
Closure of the anvil 60 from an extended position to a position in which the tissue is not compressed or is just slightly compressed can occur rapidly without causing damage to the interposed tissue. Thus, the longer-pitched thread portion 183 allows the user to quickly close the anvil 60 to the tissue in a tissue pre-compressing state. Thereafter, it is desirable to compress the tissue slowly so that the user has control to avoid over-compression of the tissue. As such, the shorter pitched thread portion 184 is used over this latter range of movement and provides the user with a greater degree of control. During such compression, the force switch 400 seen in FIG. 18 and described in co-pending U.S. Patent Provisional Application Serial No.
60/801,989 can be used to indicate to the user through the tissue compression indicator 14 (and/or to the control circuitry of the circuit board 500) that the tissue is being compressed with a force that is greater than the pre-load of the spring 420 inside the force switch 400. It is noted that FIG. 18 illustrates the force switch 400 embodiment in the normally-open configuration described as the first exemplary embodiment of U.S. Patent Provisional Application Serial No.
60/801,989. A strain gauge can also be used for measuring tissue compression.
FIGS. 19 to 23 illustrate movement of the rod 180 from an anvil-extended position (see FIGS. 19 to 20), to a 1-cm-closure-distance position (see FIG. 21), to a staple-fire-ready position (see FIG. 22), and, finally, to an anvil fully closed position (see FIG. 23).
Movement of the rod 180 is controlled electrically (via the circuit board 500) by contact between a portion of a cam surface actuator 185 on the rod 180 and actuating levers or buttons of a series of micro-switches positioned in the handle body 10.

17 A rod-fully-extended switch 610 (see FIG. 19) is positioned distal in the handle body 10 to have the actuator 185 compress the activation lever of the rod-fully-extended switch 610 when the rod 180 (and, thereby, the anvil 60) is in the fully extended position. A 1-cm switch 612 is positioned in an intermediate position within the handle body 10 (see FIGS. 20 to 21) to prevent a 1-cm cam surface portion 186 of the rod 180 from pressing the activation button of the 1-cm switch 612 when the rod 180 (and, thereby, the anvil 60) is within 1 cm of the fully closed position. After passing the 1-cm closure distance, as shown in FIG. 22, the cam surface actuator 185 engages a staple-fire-ready switch 614. The lower end of the actuator 185 as viewed in FIGS.
22 to 23 has a bevel on both the forward and rear sides with respect to the button of the staple-fire-ready switch 614 and the distance between the portion on the two bevels that actuates the button (or, only the flat portion thereof) corresponds to the acceptable staple forming range (i.e., safe firing length) of the staples in the staple cartridge 50. Thus, when the button of the staple-fire-ready switch 614 is depressed for the first time, the distance between the anvil 60 and the staple cartridge 50 is at the longest range for successfully firing and closing the staples. While the button is depressed, the separation distance 62 of the anvil 60 (see FIG. 18) remains within a safe staple-firing range. However, when the button of the staple-fife-ready switch 614 is no longer depressed -- because the actuator 185 is positioned proximally of the button, then staples will not fire because the distance is too short for therapeutic stapling. FIG. 23 show the rod 180 in the proximal-most position, which is indicated by the top end of the actuator 185 closing the lever of a rod fully-retracted switch 616. When this switch 616 is actuated, the programming in the circuit board 500 prevents the motor 120 from turning in a rod-retraction direction;
in other words, it is a stop switch for retracting the rod 180 in the proximal direction.
It is noted that FIGS. 2 to 3, 11 to 12, and 16 illustrate the distal end of the rod 180 not being connected to another device at its distal end (which would then contact the proximal end of the force switch 400). The connection band or bands between the distal end of the rod 180 and the proximal end of the force switch 400 are not shown in the drawings only for clarity purposes. In an exemplary embodiment, the pull-bands are flat and flexible to traverse the curved underside of the cartridge plunger 320 through the anvil neck 30 and up to the proximal end of the force switch 400. Of course, if the force switch 400 is not present, the bands would be connected to the proximal end of the trocar tip 410 that releasably connects to the proximal end of the anvil 60.

18 Functionality of the staple control assembly 200 is described with regard to FIGS. 12 to 16 and 24 to 27, in particular, to FIG. 24. The stapling motor 210 is held between a motor bearing 222 and a motor shaft cover 224. The axle 212 of the stapling motor 210 is rotationally connected to the proximal end of the flexible coupling 240 and the distal end of the flexible coupling 240 is rotationally connected to the proximal end of the screw 250, which rotates on bearings 260, 270, 280 that are disposed within the intermediate coupling mount 230 and the distal plate 232. The longitudinally translating nut 290 is threaded onto the screw 250 between the coupling mount 230 and the distal plate 232. Therefore, rotation of the axle 212 translates into a corresponding rotation of the screw 250.
The nut coupling bracket 300 is longitudinally fixed to the nut 290 and to the stiffening rod 310 and the firing bracket 330. The firing bracket 330 is longitudinally fixed to the cartridge plunger 320, which extends (through a non-illustrated staple driver) up to the staple cartridge 50 (or to the staples). With such a connection, longitudinal movement of the nut 290 translates into a corresponding longitudinal movement of the cartridge plunger 320. Accordingly, when the staple firing switch 22 is activated, the stapling motor 210 is caused to rotate a sufficient number of times so that the staples are completely fired from the staple cartridge 50 (and the cutting blade, if present, is extended to completely cut the tissue between the anvil 60 and the staple cartridge 50).
Programming in the circuitry, as described below, then causes the cartridge plunger 320 to retract after firing and remove any portion of the staple firing parts and/or the blade within the staple cartridge 50 from the anvil-cartridge gap 62.
Control of this stapling movement, again, occurs through micro-switches connected to the circuit board 500 through electrical connections, such as wires. A first of these control switches, the proximal staple switch 618, controls retraction of the staple control assembly 200 and defines the proximal-most position of this assembly 200. To actuate this switch, an actuation plate 306 is attached, in an adjustable manner, to a side of the nut coupling bracket 300.
See, e.g., FIGS. 6 and 24. As such, when the nut 290 moves proximally to cause the plate 306 on the nut coupling bracket 300 to activate the proximal staple switch 618, power to the stapling motor 210 is removed to stop further proximally directed movement of the staple control assembly 200.
A second of the switches for controlling movement of the staple control assembly 200 is located opposite a distal transverse surface of the stiffening rod 310. See, e.g. FIG. 27. At this surface is disposed a longitudinally adjustable cam member 312 that contacts a distal staple switch

19 620. In an exemplary embodiment, the cam member 312 is a screw that is threaded into a distal bore of the stiffening rod 310. Accordingly, when the nut 290 moves distally to cause the cam member 312 of the stiffening rod 310 to activate the distal staple switch 620, power to the stapling motor 210 is removed to stop further distally directed movement of the staple control assembly 200.
FIGS. 28 and 29 illustrate a removable connection assembly to permit replacement of a different staple cartridge 60 on the distal end of the anvil 30.
The proximal-most chamber of the handle body 10 defines a cavity for holding therein a power supply 600. This power supply 600 is connected through the circuit board 500 to the motors 120,210 and to the other electrical components of the stapler I.
The electronic components of the stapler 1 have been described in general with respect to control through the circuit board 500. The electric stapler 1 includes, as set forth above in an exemplary embodiment, two drive motors 120, 210 powered by batteries and controlled through pushbuttons 20, 21, 22. The ranges of travel of each motor 120, 210 are controlled by limit switches 610, 616, 618, 620 at the ends of travel and at intermediary locations 612, 614 along the travel. The logic by which the motors 120, 210 are controlled can be accomplished in several ways. For example, relay, or ladder logic, can be used to define the control algorithm for the motors 120,210 and switches 610, 612, 614, 616, 618, 620. Such a configuration is a simple but limited control method. A more flexible method employs a microprocessor-based control system that senses switch inputs, locks switches out, activates indicator lights, records data, provides audible feedback, drives a visual display, queries identification devices (e.g., radio frequency identification devices (RF1Ds) or cryptographic identification devices), senses forces, communicates with external devices, monitors battery life, etc. The microprocessor can be part of an integrated circuit constructed specifically for the purpose of interfacing with and controlling complex electro-mechanical systems. Examples of such chips include those offered by Atrnel, such as the Mega 128, and by PIC, such as the PIC 16F684.
A software program is required to provide control instructions to such a processor. Once fully developed, the program can be written to the processor and stored indefinitely. Such a system makes changes to the control algorithm relatively simple; changes to the software that are uploaded to the processor adjust the control and user interface without changing the wiring or mechanical layout of the device.

For a disposable device, a power-on event is a one time occurrence. In this case, the power-on can be accomplished by pulling a tab or a release that is permanently removed from the device. The removal enables battery contact, thus powering on the device.
5 In any embodiment of the device, when the device is powered on, the control program begins to execute and, prior to enabling the device for use, goes through a routine that ensures awareness of actual positions of the extend/retract and firing sub-assemblies, referred to as a homing routine. The homing routine may be executed at the manufacturer prior to shipping to the user. In such a case, the homing routine is performed, the positions of the assemblies are set, and 10 the device is shipped to the user in a ready-to-use condition. Upon power-up, the device verifies its positions and is ready to use.
Visual indicators (e.g., LEDs) are used to provide feedback to the user. In the case of the pushbutton switches 20, 21, 22, they can be lit (or backlit) when active and unlit when not active.
The indicators can blink to convey additional information to the user. In the case of a delayed 15 response after a button press, a given light can blink at an ever-increasing rate as the response becomes imminent, for example. The indicators can also light with different colors to indicate various states.
Cams are used in various locations at the stapler 1 to activate limit switches that provide position information to the processor. By using linear cams of various lengths, position ranges can

20 be set. Alternatively, encoders can be used instead of limit switches (absolute and incremental positioning). Limit switches are binary: off or on. Instead of binary input for position information, encoders (such as optical encoders) can be used to provide position information.
Another way to provide position feedback includes mounting pulse generators on the end of the motors that drive the sub-assemblies. By counting pulses, and by knowing the ratio of motor turns to linear travel, absolute position can be derived.
Use of a processor creates the ability to store data. For example, vital, pre-loaded information, such as the device serial number and software revision can be stored. Memory can also be used to record data while the stapler 1 is in use. Every button press, every limit switch transition, every aborted fire, every completed fire, etc., can be stored for later retrieval and diagnosis. Data can be retrieved through a programming port or wirelessly. In an exemplary embodiment, the device can be put into diagnostic mode through a series of button presses. In this diagnostic mode, a technician can query the stapler 1 for certain data or to transmit/output certain

21 data. Response from the stapler 1 to such a query can be in the form of blinking LEDs, or, in the case of a device with a display, visual character data, or can be electronic data. As set forth above, a strain gauge can be used for analog output and to provide an acceptable strain band.
Alternatively, addition of a second spring and support components can set this band mechanically.
An exemplary control algorithm for a single fire stapler 1 can include the following steps:
o Power on.
o Verify home position and go to home position, if necessary/desired.
o Enable extend/retract buttons (lit) and disable (unlit) staple fire button.
o Enable staple fire button only after full extension (anvil removal) and subsequent retraction with extend/retract buttons remaining enabled.
o Upon actuation of staple fire button, retract anvil until force switch is activated.
o Begin countdown by blinking fire button LED and increase blink rate as firing cycle becomes imminent. Continue monitoring of force switch and retract anvil so that force switch remains activated.
o During staple fire cycle, any button press aborts staple fire routine.
o If abort occurs before staple firing motor is activated, firing cycle stops, anvil is extended to home position, and staple fire button remains active and ready for a re-fire.
o Alternatively, if the abort occurs during movement of firing motor, firing cycle stops, firing motor is retracted, anvil is returned to home position, and firing button is rendered inactive. Accordingly, stapler (or that staple cartridge) cannot be used.
o After countdown to fire is complete, staple range limit switch is queried for position. If staple range limit switch is activated -- meaning that anvil is within an acceptable staple firing range -- then staple firing motor is activated and firing cycle proceeds. If staple range limit switch is not activated, then firing cycle is aborted, anvil is returned to home position, and staple firing button remains active ready for a re-fire attempt.
o After a completed staple firing, anvil remains in closed position and only the extend button remains active. Once anvil is extended to at least the home

22 position, both extend and retract buttons are made active. Staple fire button remains inactive after a completed staple firing.
Throughout the above exemplary cycle, button presses, switch positions, aborts, and/or fires can be recorded.
In a surgical procedure, the stapler is a one-way device. In the test mode, however, the test user needs to have the ability to move the trocar 410 and anvil 60 back and forth as desired. The power-on feature permits entry by the user into a manual mode for testing purposes. This test mode can be disengaged and the stapler reset to the use mode for packaging and shipment.
For packaging, it is desirable (but not necessary) to have the anvil 60 be disposed at a distance from the staple cartridge 50. Therefore, a homing sequence can be programmed to place the anvil 60 one centimeter (for example) away from the staple cartridge 50 before powering down for packaging and shipment.
When the electric stapler is unpackaged and ready to be used for surgery, the user turns the stapler on (switch 12). Staples should not be allowed to fire at any time prior to being in a proper staple-firing position and a desired tissue compression state. Thus, the anvilltrocar extend/retract function is the only function that is enabled. In this state, the extend and retract buttons 20,21 are lit and the staple firing switch 22 is not lit (i.e., disabled).
Before use inside the patient, the trocar 410 is extended and the anvil 60 is removed. If the stapler is being used to anastomose a colon, for example, the trocar 410 is refracted back into the anvil neck 30 and the staple cartridge 50 and anvil neck 30 are inserted trans-anally into the colon to a downstream side of the dissection. The anvil 60, in contrast, is inserted through an upstream laparoscopic incision and placed at the upstream side of the dissection. The anvil 60 is attached to the trocar 410 and the two parts are retracted towards the staple cartridge 50 until a staple ready condition occurs. As set forth above, the anvil is moved to a distance that does not substantially compress and, specifically, does not desiccate, the tissue therebetween. At this point, staple firing can occur when desired.
The staple firing sequence is started by activating the staple fire switch 22.
Staple firing can be aborted anytime during the firing sequence, whether prior to movement (during the blanching cycle) or during movement (whether the staples have started to form or not). The software is programmed to begin a staple firing countdown sequence because it is understood that

23 the tissue needs to be compressed and allowed to desiccate before staple firing should occur.
Thus, after the staple firing switch 22 is activated, the anvil 60 closes upon the interposed tissue and begins to compress the tissue. The staple firing sequence includes an optimal tissue compression (OTC) measurement and a feedback control mechanism that causes staples to be fired only when the compression is in a desired pressure range, referred to as the OTC range, and a sufficient time period has elapsed to allow fluid removal from the compressed tissue. The OTC
range is known beforehand based upon known characteristics of the tissue that is to be compressed between the anvil 60 and the staple cartridge 50 (the force switch can be tuned for different tissue OTC ranges). It is the force switch 400 that provides the OTC measurement and supplies the microprocessor with information indicating that the OTC for that particular tissue has been reached. The OTC state can be indicated to the user with an LED, for example.
When the firing sequence begins, the staple fire switch 22 can be made to blink at a given rate and then proceed to blink faster and faster, for example, until firing occurs. If no abort is triggered during this wait time, the OTC state will remain for the preprogrammed desiccation duration and staple filing will occur after the countdown concludes. In the example of colon anastomosis with a circular stapler, stapling of the dissection occurs simultaneously with a cutting of tissue at the center of the dissection. This cutting guarantees a clear opening in the middle of the circular ring of staples sufficient to create an opening for normal colon behavior after the surgery is concluded.
As the liquid from the interposed compressed tissue is removed, the compressive force on the tissue naturally reduces. In some instances, this reduction can be outside the OTC range.
Therefore, the program includes closed-loop anvil-compression control that is dependent upon continuous measurements provided by the force switch 400. With this feedback, the compressed tissue is kept within the OTC range throughout the procedure and even after being desiccated.
During the staple firing cycle, any actuation of a control switch by the user can be programmed to abort the staple fire routine. If an abort occurs before the staple firing motor 210 is activated, the firing cycle stops, the anvil 60 is extended to a home position, and the staple fire switch 22 remains active and ready for a re-fire attempt, if desired.
Alternatively, if the abort occurs during movement of the staple firing motor 210, the firing cycle stops and the staple firing motor 210 is caused to extend the anvil 60 to its home position. At this point, the staple firing

24 switch 22 is rendered inactive. Accordingly, the stapler (or that particular staple cartridge) can no longer be used (unless the staple cartridge is replaced).
It is noted that before a staple firing can occur, a staple range limit switch is queried for relative position of the staple cartridge 50 and anvil 60. If the staple range limit switch is activated ¨ meaning that anvil 60 is within an acceptable staple firing range -- then the staple firing motor 210 can be made active and the firing cycle can be allowed to proceed. If the staple range limit switch is not activated, then the firing cycle is aborted, the anvil 60 is returned to the home position, and the staple firing switch 22 remains active and ready for a re-tire attempt.
Powering (also referred to as actuating, powering, controlling, or activating) of the motor and/or the drive train of any portion of the end effector (e.g., anvil or stapler/cutter) is described herein. It is to be understood that such powering need not be limited to a single press of an actuation button by the user nor is the powering of a motor limited to a single energizing of the motor by the power supply. Control of any motor in the device can require the user to press an actuation button a number of times, for example, a first time to actuate a portion of the end effector for a first third of movement, a second time for a second third of movement, and a third time for a last third of movement More specifically for a surgical stapler, a first exemplary actuation can move the staple sled or blade past the lock-out, a second exemplary actuation can move the part up to the tissue, and a third exemplary actuation can move the sled past all staples to the end of the staple cartridge. Similarly, powering of a motor need not be constant, for example, where the motor is energized constantly from the time that the blade begins movement until it reaches the end point of its movement. Instead, the motor can be operated in a pulsed mode, a first example of which includes periodically switching on and off the power supplied by the power supply to the motor during actuation of an end effector function. More specifically for a stapler, the motor can be pulsed ten times/second as the staple/cutter moves from its proximal/start position to its distal-most position. This pulsing can be directly controlled or controlled by microprocessor, either of which can have an adjustable pulse rate.
Alternatively, or additionally, the motor can be operated with a pulse modulation (pulse-width or pulse-frequency), with pulses occurring at very short time periods (e.g., tenths, hundredths, thousandths, or millionths of a second). Accordingly, when the power supply, the motor, and/or the drive train are described herein as being powered, any of these and other possible modes of operation are envisioned and included.

After a completed staple firing, the anvil 60 remains in the closed position and only the extend switch 20 remains active (all other switches are deactivated). Once the anvil 60 is extended to at least the home position, both the extend and retract switches 20, 21 are made active 5 but the retraction switch 21 does not permit closure of the anvil 60 past the home position. The staple fire switch 22 remains inactive after a completed staple firing.
As set forth above, the anvil neck 30 houses a linear force switch 400 connected to the trocar 410. This switch 400 is calibrated to activate when a given tensile load is applied. The given load is set to correspond to a desired pressure that is to be applied to the particular tissue 10 before stapling can occur. Interfacing this switch 400 with the processor can ensure that the firing of staples only occurs within the OTC range.
The following text is an exemplary embodiment of a program listing for carrying out the methods according to the invention as described herein. The text that follows is only submitted as exemplary and those of skill in the art can appreciate that programming the methods according to 15 the invention can take many different forms to achieve the same functionality.
'Circular Stapler Program using the rev 3c board (cb280 chipset) V8.03 (CS-3c-080306.CUL) '8-3-06 'Modified program to abort with only fire button, added pbcount variable 20 'Added PWM ramping '7-28-06 'final tweaks - stan is now an integer etc.
'7-17-06 This version written for the 3c board.
'7-14 DEBUGGING VERSION

25 'Program written for 3c board using the Cubloc 280 chipset 'Note: this program is a modified version of the ones noted below. All changes not related to the addition of the E/R limit switches 'apply. The programs below were written to deal with the "gray logic" of the 1 cm switch. This version uses 'a limit switch at either end of the extend/retract stage.
'16.20 Final Version of Gray Logic program as used in prototype 0, serial number 100 T6.05

26 'modified the extend to cm 1 and retract to cm 1 routines to make sure that when they are called that they move the motor until the cm 'switch is closed; ie: When the anvil is all the way out and the retract button is pressed, retract the anvil until the cm limit switch 'is closed regardless of whether the retract button is released before the cm switch is closed. Same change for when the anvil is 'extended from the 1 cm position.
'made changes to comments in the extend/retract routines V6.02 'added loop requiring the release of both buttons to exit jog routine, and a 1 second delay at the end of jog subroutine before 'going back to main routine 'reformatted datadump labels 'added variables for high and low speed pwm values 'added extend only capability at end of completed fire to prevent crushing stapled tissue 'NOT WORKING- REMOVED added checks To ensure I cm switch Is made when extending Or retracting from the 1 cm And fully extended positions respectively 1/6.01 'All prior versions were made for testing the program on the Cubloc development board. All outputs were pulled LOW. The actual device 'requires all the outputs to be pulled high (+5V). This version is set-up to run on the actual device.
'limited the values of the EEPROM data to 255 max 'added delays before changes in motor direction, made program run smoother 'removed pwmoff commands. They were not allowing the motors to stay on when changing subroutines (for some reason) V5.27 'added the recording of jog routine button presses 'added the recording of datadump requests TV5.26

27 'added the recording of Extend/Retract button presses 'added serial number field in eeprom 'the datadump routine now keeps running total of data as it is read from eeprom 'V5.25 (circular-stapler-5-25.cul) 'added code to allow storage of data each power on cycle in eeprom TV5.24 works well, no known bugs (circular-stapler-5-24.cul) 'KMS Medical LLC (c) 2006 'MAP
T10 Extend Button Pll Retract Button P12 Fire Button P13 Extend Limit T)14 Retract Limit 'P15 Fire Forward Limit P16 Fire Back Limit P17 1 cm Limit Switch 'P18 Staple Range Limit Switch 'P19 Force Switch P20 Extend Button LED
'P21 Retract Button LED
'1122 Fire Button LED
'P23 Force LED (blue) 'P24 Not USED
1P25 Not USED
1)26 Not USED
'P27 Not USED
'P28 Not USED
'P29 Staple Range LED (green)

28 Const Device-0)280 'Comfile Tech. Cubloc CB280 claipset Dim ver As String*?
vez="3C-8.03" 'set software version here Dim extendbutton As Byte Dim retractbutton As Byte Dim firebutton As Byte Dim firstout As Byte Dim firstback As Byte Dim crnstatus As Byte 'lcm limit switch status Dim srstatus As Byte 'staplerange limit switch status Dim x As Integer Dim powerons As Byte 'store in eeprom address 2 Dim cycmunfires As Byte 'store in eeprom (powerons*5) Dim cycabortfires As Byte 'store in eeprom (powerons*5)+1 Dim cycers As Byte 'store in eeprom, number of cycle extend/retract presses Dim cycjogs As Byte Dim arm As Byte Dim completefire As Byte Dim staplerangestatus As Byte Dim bail As Byte Dim ds As Integer 'eeprom data start location for individual cycle data writing Dim fast As Integer Dim slow As Integer Dim extendonly As Byte Dim extlimit As Byte Dim retlimit As Byte Dim speed As Integer Dim dracula As Byte initalize outputs

29 Out 20,0 'extend button LED
Out 21,0 'retract button led Out 22,0 'fire button led Out 23,0 'force led Out 29,0 'staple range led 'initialize variables firstout=0 firstback4 completefire arml cycnumfires4 cycabortfires=0 cycers=0 cycjogs=0 extendonly 'CHANGE PWM VALUES HERE
fast=60000 'highspeed pwm value slow=60000 lowspeed pwm value speed=0 Output 5 'turns on pwm output for PINCH
Output 6 'turns on pwm output for FIRE
'read totals from eeprom powerons=Eeread(2,1) Incr powerons 'increment total power on number If powerons>=255 Then powerons=255 limit number of recorded powerons to an integer of one byte max Eewrite 2,powerons,1 'write total power on number to eeprom 5 ds=powerons*5 'JOG and DATADUNT Check 'push any button within 2 (or so) seconds to go to jog routine 'hold all three buttons on at startup to dump the data 10 For x=1 To 50 If Keyin(10,20)=0 And Keyin(11,20)=0 And Keyin(1Z20)=0 Then datadump 'write all stored data to the debug screen Exit For Elscif Keyin(10,20)=0 Or Keyin(11,20)=0 Or Keyni(12,20)=0 Then 'either e/r button or 15 the fire button pressed jog Exit For End If Delay 20 20 Next 'HOMING SEQUENCES
25 cmstatus=Keyin(17,20) 'read the status of the lcm limit switch If =status-0 Then homeretract Elseif emstatus=1 Then

30 homeextend End If

31.
'Return fire motor to back position homefire 'this returns the fire motor to the full retracted condition (P6 limit switch) t******************************************************************************

**********
'Main Loop t******************************************************************************

0 **********
Do Debug "Main Loop",Cr Delay 1000 anstatus¨Keyin(17,20) 'read the 1 cm switch istaplerangestatus=-Keyin(5,20) 'read the staplerange limit switch extendbutton=Keyin(10,20) retractbutton=Keyin(11,20) firebutton=Keyin(12,20) If cmstatus=0 And Keyin(13,20)=c>0 Then Out 20,1 'turn extend led on Out 21,1 'turn retract led on Elseif cmstatus=0 And Keyin(13,20)=0 Then Out 20,0 'turn off extend led because extend limit met Out 21,1 'turn on retract limit Elseif cmstatus=1 Then Out 20,1 Out 21,0 End If

32 'check firebutton led status If firstout=1 And firstback=1 And arm=1 And completefire<>1 And cmstatus<>0 Then Out 22,1 'turn on fire button led Else Out 22,0 'turn off fire led End If 'check for extend retract button press If extendbutton=0 And cmstatus=0 Then extend Elseif cmstatus-1 And extendbutton Then extend End If If retractbutton=0 And cmstatus=0 Then 'And extendonly=0 retract End If 'check for firebutton press If firebutton=0 And firstout=1 And firstba,ck=1 And arm=1 And completefire<>1 And cmstatus<>0 Then initialfire Loop 'keep looping til powerdown End 'End of program 1************************************************************************
' SUBROUTINES

33 1************************************************************************
t_ ......
'HOME: retract to cm switch=not pressed Sub homeretractO 'retract until 1 cm switch is open Debug "Homeretract",Cr 'Delay 1000 Pwm 0,slow,60000 Do Until Keyin(17,20)=1 'retract until 1 cm switch is open Out 31,1 'ER motor reverse Loop Out 31,0 'er motor off Out 21,0 'turn retract led Off Out 20,1 'turn extend led On Pwinoff 0 'turn pwrn off End Sub ' _______ 'HOME: extend to cm switch=pressed Sub homeextendo 'extend until 1 cm switch is closed Debug "Homextend",Cr 'Delay 1000 Pwm 0,slow,60000 If Keyin(17,20)=1 Then Do Until Keyin(17,20).--1) 'now the 1 cm switch is pressed Out 30,1 'ER motor forward DDD
Loop End If

34 Out 30,0 DDD
Pwmoff Delay 300 homeretract 'once the switch is made, call homeretract End Sub 'Fire motor homing routine Sub homefire0 Debug "Homefire",Cr Delay 1000 Pwm 1,slow,60000 Do Until Keyin(16,20)=-0 'retract firing stage until back switch is closed Out 33,1 Loop Out 33,0 Pwmoff 1 End Sub =
-----------------'JOG Routine Sub jog() Out 20,1 Out 21,1 Do Delay 25 If Keyin(10,20)=0 And Keyin(11,20)=0 Then Exit Do 'if both buttons pressed, exit jog routine and start homing routine after 1 second delay 5 If Keyin(10,20) And Keyin(11,20)<>0 And Keyin(12,20).c>0 Then Pwm 0,slow,60000 'Out 30,1 'extend motor forward Do Until Keyin(10,20)<>0 Or Keyin(13,20)=0 Out 30,1 'extend motor on forward DDD
10 Loop Out 30,0 'extend motor off forward DDD
Pwmoff 0 Incr cycjogs If cycjogs>=255 Then cycjogs=255 15 Eewrite ds+3,cycjogs,1 End If If Keyin(1 I ,20)O And Keyin(10,20)<>0 And Keyin(12,20)<>0 Then Pwm 0,slow,60000 20 Do Until Keyin(11,20)<>0 Or Keyin(14,20)=0 Out 31,1 'extend motor reverse Loop Out 31,0 'extend motor off reverse Pwmoff 0 25 Incr cycjogs If cycjogs>=255 Then cycjogs=255 Eewrite ds+3,cycjogs,1 End If 30 If Keyin(12,20)=0 And Keyin(10,20)-0 Then jog the fire motor forward Pwm 1,slow,60000 Do Until Keyin(10,20)<>0 Or Keyin(12,20)<>0 Or Keyin(15,20)=0 Out 32,1 'fire motor forward Loop Out 32,0 'fire motor off forward Pwmoff 1 Incr cycjogs cycjogs>=255 Then cycjogs=255 Eewrite ds+3,cycjogs,1 End If If Keyin(12,20)=0 And Keyin(11,20)4 Then 'jog the fire motor reverse Pwm 1,slow,60000 Do Until Keyin(11,20)<>0 Or Keyin(12,20)<>0 Or Keyin(16,20)=0 Out 33,1 'fire motor reverse Loop Out 33,0 'fire motor off reverse Pwmoff I
Incr cycjogs If cycjogs>=255 Then cycjogs=255 Eewrite ds+3,cycjogs,1 End If Loop Do Until Keyin(10,20)--1 And Keyin(11,20)=1 let off both buttons before exiting jog routine Delay 10 Loop Out 20,0 'turn on eh button leds Out 21,0 Delay 1000 End Sub 'Extend until extend limit is met Sub extend() Out 22,0 'turn off fire button led while extending Out 21,0 'turn off retract button led while extending Pwm 0,fast,60000 Do Until Keyin(10,20)=1 Or Keyin(13,20)=0 'extend until either the extend limit is closed or the extend button is released Out 30,1 'ER motor forward DDD
Loop Out 30,0 DDD
If firstout=0 Then 'this will keep the extend motor going on the first extension until the anvil is all the way out Do Until Keyin(13,20)=0 Out 30,1 DDD
Loop End If Out 30,0 'DDD
Pwmoff 0 Incr cycers If cycers>=255 Then cycers=255 Eewrite ds-1-2,cycers,1 If Keyin(13,20)=0 Then firstout---1 'set the firstout flag to enable fire button Out 20,0 'turn off extend led End If End Sub 'Retract until cm switch is open Sub retract() Out 22,0 'turn off fire button led while retracting Out 20,0 'turn off extend button led while retracting Pwm 0,fast,60000 Do Until Keyin(11,20)=1 Or Keyin(17,20)=1 'retract until either the lcm switch goes open or the extend button is released Out 31,1 'ER motor reverse Loop Out 31,0 Pwmoff 0 Incr cycers If cycers>=255 Then cycers=255 Eewrite ds+2,cycers,1 If Keyin(17,20)=1 Then firstback=1 Out 21,0 'turn retract led off End If If firstout=1 And firstback---1 Then arm=1 'set the arm flag to arm the fire button End Sub 'DATADUIVLP Routine Sub datailump() Dim chef As Byte Dim tf As Byte 'total fires Dim fa As Byte 'total aborts Dim ers As Integer Dim tj As Byte Dim tdd As Byte Dim stan As Integer Dim kyle As Byte Dim token As Byte Dim ike As Byte Dim kenny As Byte Dim sn As Byte ta=0 ers., ti=0 tdd=0 Eewrite ds+4,1,1 'write 1 to the ds+4 eeprom register denoting that datadump was accessed Delay 1000 sn=Eeread(0,1) Debug "Circular Stapler Stored Data",Cr Debug "Version ",ver,Cr Debug "ICMS Medical LLC",Cr Debug " 1,,cr Debug Cr Debug "Serial Number: ",Dec sn,Cr powerons=Eeread(2,1) If powerons>=255 Then powerons=255 Debug "Total Cycles: ",Dec powerons,Cr Debug Cr Debug" ___________________ ",Cr Debug Cr For stan=5 To (powerons*5) Step 5 Debug "Cycle ",Dec (stan/5),Cr 5 Debug" --------------- ",Cr chef¨Eeread(stan,1) tf=chef+tf Debug "Completed Fires: ",Dec chef,Cr kyle=F-eread(stan+1,1) 10 ta=kyle+ta Debug "Aborted Fires: ",Dec kyle,Cr token=Eeread(stan+2,1) ers=token+ers Debug "E/Rs: ",Dec token,Cr 15 ike=Eeread(stan+3,1) tj=ae+tj Debug "Jogs: ",Dec ilce,Cr kenny=Eeread(stan+4,1) tdd=kenny+tdd 20 Debug "Datadumps: ",Dec kenny,Cr Debug Cr Next 'stan Debug" ------------------- ",Cr 25 Debug "Cycle Totals",Cr Debug Cr Debug "Completed Fires: ",Dec tf,Cr Debug "Aborted Fires: ",Dec ta,Cr Debug "E/R Presses: ",Dec ers,Cr 30 Debug "Jog Presses: ",Dec tj,Cr Debug "Datadumps: ",Dec tdd,Cr Debug Cr Delay 1000 For x=1 To ft blink the number of completed firing cycles Out 22,1 Delay 500 Out 22,0 Delay 500 Next 'x Do Until Adin(0)>800 And Keyin(3,20)=1 'wait until datadump buttons are released Loop End Sub 'Initial fire Sub initialfire() Dim FM Integer Dim p As Integer Dim t As Integer Dim y As Integer Dim z As Integer Dim q As Integer Dim timmy As Integer Dim butter As Integer Dim numblinlcs As Integer Dim fbcount As Integer Debug clr,Cr 'turn off extend and retract buttons to show that they are not active for abort?
Out 20,0 'extend button Out 21,0 'retract button t=15 'total blink time p=3 'number of blink periods Pwrn 0,fast,60000 'start blink and adjust pinch motor to force f=(t*1000)/p fbcount=0 If Keyin(12,20)=1 Then fbcount=1 For y=1 lop numblinks= (t*y)/p For z=1 To numblinlcs timmy=f/numblinIcs butter¨timmy/50 'calibrate this to seconds If timm.30 Then timmy=1 If Keyin(12,20)=0 And fbcount=1 Then bail=1 'set abortfire flag Exit For End If If Keyin(12,20)=1 Then fbcount=1 Do Until Keyin(19,20) Or Keyin(14,20)=0 'retract until force switch met or retract limit met Out 31,1 If Keyin(12,20)=0 And fbcount=1 Then bail=1 'set abortfire flag Exit Do End If If Keyin(12,20)=1 Then fbcount----1 Loop If bail=1 Then Exit For Out 31,0 Out 23,1 'force led Out 22,1 'fire button led For q=0 To butter Delay 10 If Keyin(12,20)=0 And fbcount=1 Then bai1=1 'set abortfire flag Exit For End If If Keyin(12,20)=1 Then fbcount=1 If Keyin(19,20)=1 Then Out 23,0 Next 'q If bail=1 Then Exit For Do Until Keyin(1 9,20)=0 Or Keyin(14,20)=0 'retract until force switch met or retract limit met Out 31,1 If Keyin(12,20)=O And fbcount,--1 Then bail=1 'set abortfire flag Exit Do End If If Keyin(12,20)=1 Then fbc,ount=1 Loop Out 31,0 Out 23,1 If Keyin(12,20)=0 And fbcount=1 Then bai1=1 'set abortfire flag Exit For End If If Keyin(12,20)=1 Then fbcount=1 Out 22,0 For q=0 To butter Delay 10 If Keyin(12,20)---0 And fbcount=1 Then bail=1 'set abortfire flag Exit For End If If Keyin(12,20)=1 Then fbcount=1 If Keyin(19,20)=1 Then Out 23,0 Next 'q If bait=1 Then Exit For Next 'z 'Debug Dec? fbcount,Cr If bail=1 Then Exit For Next 'y Pwmoff 0 If bail=1 Then abortfire Else istaplerangeeheck final ire End If End Sub 'Staple Range Check Routine 5 Sub staplerangecheck() srstatus=Keyin(29,20) 'read the staplerartge limit switch If srstatus) Then finalfire Else 10 abortfire End If End Sub 15 'Final Fire Routine Sub finalfire() Out 23,0 'turn force led off 20 Out 20,0 'turn extend led off Out 21,0 'turn retract led off Out 22,1 'Turn on fire led to signify final fire abort ready Pvirnoff 1 Pvvm 1,fast,60000 25 'Out 32,1 'fire motor forward DDD
completefire--1 Do Until Keyin(15,20)=0 'fire forward until forward limit is met If speed>0000 Then speed=60000 If speed<60000 Then 30 speed=speed+10000 End If Pwm 1,speed,60000 Out 32,1 Delay 50 If Keyin(12,20)=0 Then Or Keyin(10,20)=0 Or Keyin(11,20)=0 bail=1 Exit Do End If Loop Out 32,0 'fire motor fwd off DDD
speed=0 Delay 250 Do Until Keyin(16,20)A) 'retract fire motor If speed>50000 Then speed0000 If speed<60000 Then speed=speed+10000 End If Pwm 1,speed,60000 Out 33,1 Delay 50 Loop speed=0 Out 33,0 Pw-moff 1 Out 22,0 'turn fire led off Out 21,0 'turn off retract led extendonly=1 Incr cycnumfires If cycnumfires>=255 Then cycnumfires=255 Eewrite ds,cycnumfires,1 'write the current cycle number of fires to the eeprom Delay 200 End Sub 'return to the main routine 'Abort fire Sub abortfire0 Debug "Fire aborted before firingli",Cr Out 31,0 'turn retract motor off Out 32,0 'turn fire forward off DDD
Out 23,0 'turn force led off Pwm 1,fast,60000 Delay 250 Do Until Keyin(1 6,20)=0 'retract fire motor Out 33,1 Loop Out 33,0 Pwmoff 1 Out 22,0 'turn fire led off Incr cycabortfires If cycabortfires>=255 Then cycabortfires=-255 Eewrite ds+1,cycabortures,1 'write the current cycle abortfires to the eeprom Delay 200 homeextend 'extend to lcm End Sub Also mentioned above is the possibility of using identification devices with removable and/or interchangeable portions of the end effector. Such identification devices, for example, can be used to track usage and inventory.
One exemplary identification device employs radio-frequency and is referred to as an RFID. In an exemplary embodiment where a medical stapler uses re-loadable, interchangeable staple cartridges, such as the stapler 1 described herein, an RED can be placed in the staple cartridge to ensure compatibility with the particular stapler and an RFID
reader for sensing compatible staple cartridges can be associated with the handle. In such a configuration, the reader interrogates the RFID mounted in the cartridge. The RFD responds with a unique code that the stapler verifies. If the stapler cartridge is labeled as verified, the stapler becomes active and ready for use. If the cartridge is rejected, however, the stapler gives a rejected indication (e.g., a blinking LED, an audible cue, a visual indicator). To avoid accidental or improper reading of a nearby staple cartridge, the antenna of the RF1D reader can be constructed to only read the RFID
when the staple cartridge is installed in the stapler or is very nearby (optimally, at the distal end of the device). Use of the RF1D can be combined with a mechanical lockout to ensure that only one fire cycle is allowed per staple cartridge. RFIDs have drawbacks because the readers are expensive, the antennas are required to be relatively large, and the distance for reading is relatively close, typically measured in centimeters.
Other wireless authentication measures can be employed. Active RFIDs can be used.
Similarly, infrared (IR) transmission devices can be used. However, both of these require the generation of power at the receiving end, which is a cost and size disadvantage.
Another exemplary identification device employs encryption. With encryption comes the need for processing numbers and, associated with such calculations, is use of processing chips (e.g., a microprocessor), one of which is to be placed on the interchangeable part, such as a staple cartridge or a replaceable end effector shaft Such encryption chips have certain characteristics that can be analyzed for optimization with the surgical instrument of the present invention. First, a separate power source for the interchangeable part is not desired. Not only would such a power source add cost, it would also add undesirable weight and take up space that is needed for other features or is just not available. Thus, power supply to the part should come from the already existing power supply within the handle. Also, supply of power should be insured at all times.
Because the interchangeable part is relatively small, the encryption chip should be correspondingly small. Further, both the handle and the interchangeable part are configured to be disposable, therefore, both encryption processors should have a cost that allows disposability.
Finally, connections between the encryption device on the interchangeable part and the corresponding encryption device on the handle should be minimized. As will be discussed below, the encryption device according to the present invention provides all of these desirable characteristics and limits the undesirable ones.
Devices for encrypted identification are commercially available. One of such encryption devices is produced by Dallas Semiconductor and is referred to as the DS2432 chip. The DS2432 chip not only provides encrypted identification between a reader and a transponder, but it also has a memory that can be used to store device-specific information, which information and its uses will be described in further detail below. One beneficial characteristic of the DS2432 is that it is a 1-wire device. This means that the power and both of the input and output signals travel on the same line. With a 1-wire device such as the DS2432, there is only the need for a single wire to traverse the distance from the handle body 10 through the anvil neck 30 to the interchangeable staple cartridge 50 in order to make a connection between the handle and the end effector. This configuration satisfies the characteristic of having a minimal amount of electrical connections and has a correspondingly reduced cost for manufacture. It is true that the DS2432 chip requires ground, however, the metallic anvil neck 30 is electrically conducting and is connected to ground of the device 1, therefore, an exemplary embodiment for the ground connection of the DS2432 chip is made by direct electrical contact through a lead to the neck 30 or by directly connecting the chip's ground to the neck 30.
One exemplary encryption circuit configuration places a first encryption chip on the interchangeable part (e.g., the staple cartridge). Ground for the first encryption chip is electrically connected to a metallic portion of the interchangeable part which, in turn, is electrically connected to ground of the device, for example, to the neck 30. The 1-wire connection of the DS2432 chip is electrically connected to a contact pad that is somewhere on the interchangeable part but is electrically disconnected from ground. For example, if the interchangeable part is a linear 60 mm staple cartridge, the DS2432 can be attached to or embedded within the electrically insulated distal end of the cartridge distal of the last staple set The encryption chip can be embedded on a side of the cartridge opposite the staple ejection face so that it is neither exposed to the working surfaces nor to the exposed tissue when in use. The ground lead of the DS2432 chip can be electrically connected to the metallic outer frame of the staple cartridge, which is electrically connected to ground of the stapler. The 1-wire lead is electrically connected to a first conductive device (such as a pad, a lead, or a boss) that is electrically insulated from the metallic frame of the cartridge. A
single electrically conductive but insulated wire is connected at the proximal end to the circuit hoard or to the appropriate control electronics within the handle of the device. This wire is insulated from electrical contact with any other part of the stapler, especially the grounded frame, and travels from the handle, through the neck and up to the receiving chamber for the 5 interchangeable part. At the distal end, the insulated wire is exposed and electrically connected to a second conductive device (such as a pad, a lead, or a boss) that is shaped to positively contact the first conductive device on the cartridge when the cartridge is locked into place in the end effector. In such a configuration, the two conductive devices form a direct electrical connection every time that the interchangeable part (e.g., the staple cartridge) is inserted within the end 10 effector; in one particular embodiment, contact can be made only when the part is correctly inserted.
The DS2432 is also only a few square millimeters in area, making the chip easy to install on a small interchangeable part, such as a staple cartridge, while simultaneously satisfying the minimal size requirement. It is noted that the DS2432 chip is relatively inexpensive. To keep all 15 communication with the DS2432 chip hidden from outside examination, a DS2460 (also manufactured by Dallas Semiconductor) can be used to perform a comparison of an encrypted transmission received from a DS2432 with an expected result calculated internally. The characteristics of both of these chips are explained, for example, by Dallas Semiconductors' Application Note 3675, which is hereby incorporated by reference herein in its entirety. The 20 DS2460 chip costs significantly more than the DS2432 chip, but is still inexpensive enough to be disposed along with the handle. It is noted that the number of disposable interchangeable parts of medical devices (such as the surgical instrument of the present invention) typically outnumber the handle that receives the interchangeable parts by a significant amount.
Accordingly, if the DS2432 chip is placed in the interchangeable part and the DS2460 chip is placed in the handle, the 25 low cost encryption characteristic is satisfied. There exists an alternative circuit configuration using two DS2432 chips that is explained in FIG. 2 of Application Note 3675, which circuit eliminates the need of the more expensive DS2460 chip by performing the comparison with a local microprocessor (e.g., microprocessor 2000). In such a configuration, the cost for adding encryption into the device 1 is reduced, however, as explained, the configuration gives up some 30 aspects of security by making available to inspection both numbers that are to be compared.
The process for electronically verifying the identity of an interchangeable part on a medical device using encryption is described with an exemplary embodiment having one DS2432 chip and one DS2460 chip. The exemplary control circuit for the encryption device is shown in FIG, 30. This exemplary embodiment is described using a linear stapler having a handle containing therein a circuit board with a microprocessor 2000. One free I/0 pin 2010 of the microprocessor 2000 is connected to a first lead 2110 of the DS2460 and another 110 pin 2020 is connected to a second lead 2120. Each interchangeable part 2200 is provided with a DS2432 chip and the 1-wire lead is connected to a third 1/0 pin 2030 of the microprocessor 2000.
To start the process, an interchangeable part 2200 is connected to the device, making electrical contact with ground and with the 1-wire lead. When the microprocessor 2000 detects that a new part 2200 has been connected to the device 1, it runs an authentication routine. First, the microprocessor 2000 initiates a random number request to the DS2460 over the first communication pin 2010. The DS2460 has a pre-programmed secret number that is the same as the pre-programmed secret numbers stored in each of the DS2432 chips contained on the interchangeable parts 2200. Therefore, when the same random number is provided to both the DS2432 and the DS2460 chips, the output result from each of the two chips will be identical. The DS2460 generates a random number and supplies it, via the second pin 2020, to the microprocessor 2000 for forwarding, via pin 2030, on to the DS2432 over the 1-wire lead. When the DS2432 receives the random number, it applies its SHA-1 algorithm (developed by the National Institute of Standards and Technology (N1ST)) to cryptographically generate a hash code reply. This hash code reply is transmitted back over the 1-wire lead to the microprocessor 2000 and is forwarded, via either pin 2010 or 2020 to the DS2460. During this period of time, the DS2460 is also calculating its own a hash code reply. First, the DS2460 internally applies the same random number sent to the DS2432 to its own SHA-1 algorithm and stores, internally, the generated hash code reply. The DS2460 also stores the hash code reply transmitted from the DS2432 through the microprocessor 2000. Both of the hash code replies are compared and, if they are identical, the interchangeable part 2200 is confirmed as authenticated. If there is a difference between the hash code replies, then the part 2200 is rejected and the device is placed in a state where the part 2200 either cannot be used or can be used, but only after certain safeguards are met.
For example, data regarding the time, date, environment, etc. and characteristics of the unauthenticatal part can be stored for later or simultaneous transmission to the manufacturer (or its agent) to inform the manufacturer that the user is attempting to use or has used an unauthorized part 2200 with the device. If there was no encryption in the messages, the authentication messages could be intercepted and counterfeit, pirated, or unauthorized parts 2200 could be used without having to purchase the parts 2200 from an authorized distributor. In the exemplary encryption embodiment described herein, the only information that is transmitted across lines that can be examined is a single random number and a single hash code reply. It is understood that it would take hundreds of years to decrypt this SHA-1-generated reply, thus reducing any incentive for reverse engineering.
Because the chips used in this example each have secure memories that can only be accessed after authentication occurs, they can be programmed to employ multiple secret keys each stored within the memory. For example, if the DS2460 has multiple keys stored therein and the parts 2200 each have only one key selected from this stored set of multiple keys, the DS2460 can act as a "master" key to the "general" single keys of the parts 2200.
By authenticating the interchangeable part of the surgical instrument of the present invention, many positive results are obtained. First, the instrument manufacturer can prevent a user from using unauthorized parts, thereby insuring use of only authorized parts. Not only does this guarantee that the manufacturer can receive royalties from sales of the interchangeable part, but it also allows the manufacture to insure that the quality of the surgical parts remains high.
Having the encryption circuitry contain memory dramatically enhances the benefits provided by the present invention. For example, if a single end effector of a linear stapler can receive 30 mm, 60 mm, and 120 min staple cartridges, for example, each size of the cartridges could be provided with an individualized key and the handle can be programmed to store and use each of these three keys. Upon receiving a hash code reply that corresponds to one, but not the other two internally calculated hash code replies, the handle would know what kind of cartridge has been inserted in the device. Each cartridge could also contain in its memory cartridge-specific parameters, such as staple sled movement length, that are different among the various sized cartridges and, therefore, cause the handle to behave differently dependent upon the cartridge detected.
The parameters examined can also account for revision levels in the particular part. For example, a revision 1 cartridge could have certain parameters for use and, by detecting that particular cartridge, programming could cause the handle to not allow use of revision 1 cartridges but allow use of revision 2 cartridges, or vice-versa.
Having memory on the encryption chips can also allow the cartridge to keep track of other kinds of data. For example, the cartridge can store the identity of each handle to which it was connected, the identity of the handle that fired the cartridge, the time, date and other temporal data when use and/or connection occurred, how long it took to fire the cartridge, how many times the firing trigger was actuated during staple firing, and many other similar parameters. One parameter in particular could record data when the cartridge misfires. This would allow the manufacturer to determine if the cartridge was faulty or if user-error occurred, for example, the latter being investigated to assist the.user with remedial measures or other training. By having memory available at the handle, other handle-relevant parameters could be stored, for example, duration of each procedure, speed of each staple firing, torque generated at each firing, and/or load experienced throughout each firing. The memory could be powered for years merely from the lithium-based power cells already present in the handle. Thus, longevity of handle data can be ensured. The memory can be used to store all uses of a particular handle, along with relevant calendar data For example, if a handle is only certified for use in a single surgical procedure but the handle has data indicating that staple cartridges were fired days or weeks apart, then, when it was finally returned to the manufacturer for recycling, the manufacturer could detect that the user (hospital, doctor, clinic, etc.) was improperly and, possibly, unsafely, using the handle. Encrypted authentication can be used with removable battery packs as well. Moreover, sensors can be added to any portion of the device for communicating information to be stored within the memory of the encryption chips. For example, temperature sensors can transmit operating room temperature existing when the cartridge was fired. This temperature reading can be used to determine if later infection was caused by improper temperature control existing during the procedure (e.g., in countries where air-conditioning is not available).
In the unlikely event that the stapler becomes inoperable during use, a mechanical override or bail-out is provided to allow manual removal of the device from the patient. All bailout uses can be recorded with the memory existing on these encryption chips.
Furthermore, data that could indicate why bailout was necessary could be stored for later examination. For quality assurance, when bailout is detected, the handle can be programmed to indicate that a certified letter should be sent to the customer/user informing them of the bailout use.
As described above, the present invention is not limited to a circular stapler, which has been used as an exemplary embodiment above, and can be applied to any surgical stapling head, such as a linear stapling device, for example. Accordingly, a linear stapler is being used in the text that follows for various exemplary embodiment. However, use of a linear stapler in this context should not be considered as limited only thereto.
Described above are components that exist along the staple control axis 80 of linear and circular staplers and these components form the staple control assembly 200.
As set forth therein, the required force for proper staple ejection and tissue cutting can be over 200 pounds and, possibly, up to 250 pounds. It has been determined that minimum requirements for carrying out the desired stapling and cutting functions with a linear electric surgical stapler for human tissue (such as colon tissue, for example) are:
1) delivering approximately 54.5 kg (120 pounds) of force over a stroke of about 60 mm (-2.4") in approximately 3 seconds; or 2) delivering approximately 82 kg (180 pounds) of force over a stroke of about 60 mm (-2.4") in approximately 8 seconds.
The electric-powered, hand-held linear surgical stapling device of the present invention can meet these requirements because it is optimized in a novel way as set forth below.
To generate the force necessary to meet the above-mentioned requirements, the maximum power (in watts) of the mechanical assembly needs to be calculated based upon the maximum limits of these requirements: 82 kg over 60 mm in 3 seconds. Mathematical conversion of these figures generates an approximate maximum of 16 Watts of mechanical power needed at the output of the drive train. Conversion of the electrical power into mechanical power is not 1:1 because the motor has less than 100% efficiency and because the drive train also has less than 100%
efficiency. The product of these two efficiency ratings forms the overall efficiency. The electrical power required to produce the 16 Watts of mechanical power is greater than the 16 Watts by an inverse product of the overall efficiency. Once the required electrical power can be determined, an examination of available power supplies can be made to meet the minimum power requirements. Thereafter, an examination and optimization of the different power supplies can be made. This analysis is described in detail in the following text.
Matching or optimizing the power source and the motor involves looking into the individual characteristics of both. When examining the characteristics of an electric motor, larger motors can perform a given amount work with greater efficiency than smaller motors. Also motors with rare-earth magnets or with coreless construction can deliver the same power in a smaller size, but at higher cost. Further, in general, larger motors cost less than smaller motors if both are designed to deliver the same power over a given period of time.
Larger motors, however, have an undesirable characteristic when used in surgical stapling devices because the handle in which they are to be placed is limited by the size of an operator's hand_ Physicians desire to use 5 devices that are smaller and lighter, not larger and heavier. Based upon these considerations, cost, size, and weight are factors that can be optimized for use in the surgical stapler handle of the present invention.
Available motors for use within a physician's hand include motors with relatively inexpensive ceramic magnets and motors with relatively expensive rare earth (i.e., neodymium) 10 magnets. However, the power increase of the latter as compared to the former is not sufficiently large to warrant the substantial increase in cost of the latter. Thus, ceramic magnet motors can be selected for use in the handle. Exemplary motors come in standard sizes (diameter) of 27.5 mm or 24 mm, for example. These motors have a rated efficiency of approximately 60%
(which decreases to 30% or below depending upon the size of the load). Such motors operate at speeds of 15 approximately 30,000 rpm (between 20,000 and 40,000 rpm) when unloaded.
Even though such conventional motors could be used, it would be desirable to reduce the size even further. To that effect, the inventors have discovered that coreless, brush-type, DC
motors produce similar power output but with a significant reduction in size.
For example, a 17 mm diameter coreless motor can output approximately the same Power as a standard 24 mm 20 diameter motor. Unlike a standard motor, the coreless motor can have an efficiency of up to 80%.
Coreless motors almost all use rare earth magnets.
With such a limited volume and mechanical power available, it is desirable to select a mechanical gear train having the greatest efficiency. Placing a rack and pinion assembly as the final drive train control stage places a high-efficiency end stage in the drive train as compared to a 25 screw drive because, in general, the rack and pinion has an approximate 95% efficiency, and the screw drive has a maximum of about 80% efficiency. For the linear electric stapler, there is a 60 mm travel range for the stapling/cutting mechanism when the stapler has a 60 mm cartridge (cartridges ranging from 30 mm to 100 turn can be used but 60 mm is used in this example for illustrative purposes). With this travel range, a 3-second, full travel duration places the rack and 30 pinion extension rate at 0.8 inches per second. To accomplish this with a reasonably sized rack and pinion assembly, a gear train should reduce the motor output to approximately 60 rpm. With a motor output speed of approximately 30,000 rpm, the reduction in speed for the drive train becomes approximately 500:1. To achieve this reduction with the motor, a 5-stage drive train is selected. It is known that such drive trains have an approximate 97%
efficiency for each stage.
Thus, combined with an approximate 95% efficiency of the rack and pinion, the overall efficiency of the drive train is (0.95)(0.97)5 or 82%. Combining the 60% motor efficiency with the 82%
drive train efficiency yields an overall electrical to final mechanical efficiency of approximately 49.2%. Knowing this overall efficiency rating, when determining the amount of electrical power required for operating the stapler within the desired requirements, the actual electrical power needed is almost twice the value that is calculated for producing the stapling/cutting force.
To generate the force necessary to meet the above-mentioned requirements, the power (in watts) of the mechanical assembly can be calculated based upon the 82 kg over 60 mm in 3 seconds to be approximately 16 Watts. It is known that the overall mechanical efficiency is 49.2%, so 32.5 Watts is needed from the power supply (16 mech. watts 32.5 elec. Watts x 0.492 overall efficiency.). With this minimum requirement for electrical power, the kind of cells available to power the stapler can be identified, which, in this case, include high-power Lithium Primary cells. A known characteristic of high-power Lithium cells (e.g., CR123 or CR2 cells) is that they produce about 5 peak watts of power per cell. Thus, at least six cells in series will generate the required approximate amount of 32.5 watts of electrical power, which translates into 16 watts of mechanical power. This does not end the optimization process because each type of high-power Lithium cell manufactured has different characteristics for delivering peak power and these characteristics differ for the load that is to be applied.
Various battery characteristics exist that differentiate one battery of a first manufacturer from another battery of a second manufacturer. Significant battery characteristics to compare are those that limit the power that can be obtained from a battery, a few of which include:
= type of electrolyte in the cell;
= electrolyte concentration and chemistry;
= how the anode and cathode are manufactured (both in chemistry and in mechanical construction); and = type and construction of the PTC (positive temperature coefficient of resistance) device.
Testing of one or more of these characteristics gives valuable information in the selection of the most desirable battery for use in the stapling device. It has been found that an examination of the last characteristic -- PTC device behavior -- allows an optimization of the type of battery to perform the desired work.
Most power sources are required to perform, with relative certainty and efficiency, many times throughout a long period of time. When designing and constructing a power source, it is not typical to select the power source for short-duration use combined with a low number of uses.
However, the power source of an electric stapling device is only used for a short duration and for a small number of times. In each use, the motor needs to be ready for a peak load and needs to perform without error. This means that, for surgical staplers, the stapling/cutting feature will be carried out during only one medical procedure, which has cycle counts of between 10 and 20 uses at most, with each use needing to address a possible peak load of the device.
After the one procedure, the device is taken out of commission and discarded. Therefore, the power source for the present invention needs to be constructed unlike any other traditional power supply.
The device according to the present invention is constructed to have a limited useful life of a power cell as compared to an expected useful life of the power cell when not used in the device.
When so configured, the device is intended to work few times after this defined "life span." It is known that self-contained power supplies, such as batteries, have the ability to recover after some kind of use. For optimization with the present invention, the device is constructed within certain parameters that, for a defined procedure, will perform accordingly but will be limited or unable to continue performance if the time of use extends past the procedure. Even though the device might recover and possibly be used again in a different procedure, the device is designed to use the power cells such that they will most likely not be able to perform at the enhanced level much outside the range of intended single use periods or outside the range of aggregate use time. With this in mind, a useful life or clinical life of the power supply or of the device is defined, which life can also be described as an intended use. It is understood that this useful/clinical life does not include periods or occurrences of use during a testing period thereof to make sure that the device works as intended. The life also does not include other times that the device is activated outside the intended procedure, i.e., when it is not activated in accordance with a surgical procedure.
Conventional batteries available in the market are designed to be used in two ways: (1) provide a significant amount of power for a short duration (such as in a high-drain digital device like cameras) or (2) provide a small amount of power over a long duration (such as a computer's clock backup). If either of these operations is not followed, then the battery begins to heat up. If left unchecked, the battery could heat to a point where the chemicals could cause significant damage, such as an explosion. As is apparent, battery explosion is to be avoided. These extremes are prevented in conventional batteries with the presence of the PTC device ¨
a device that is constructed to limit conduction of the battery as the battery increases in temperature (i.e., a positive temperature coefficient of resistance). The PTC device protects batteries and/or circuits from overcurrent and overtemperature conditions. Significantly, the PTC device protects a battery from external short circuits while still allowing the battery to continue functioning after the short circuit is removed. Sonic batteries provide short-circuit and/or overtemperature protection using a one-time fuse. However, an accidental short-circuit of such a fused battery causes the fuse to open, rendering the battery useless. PTC-protected batteries have an advantage over fused batteries because they are able to automatically "reset" when the short circuit is removed, allowing the battery to resume its normal operation. Understanding characteristics of the PTC device is particularly important in the present invention because the motor will be drawing several times greater current than would ever be seen in a typical high-drain application.
The PTC device is provided in series with the anode and cathode and is made of a partially conducting layer sandwiched between two conductive layers, for example. The device is in a low-resistance condition at a temperature during a normal operation (depending on circuit conditions in which the device is used, for example, from room temperature to 40 C.). On exposure to high temperature due to, for example, unusually large current resulting from the formation of a short circuit or excessive discharge (depending on circuit conditions in which the device is used, for example, from 60 to 130 C), the PTC device switches into an extremely high-resistance mode.
Simply put, when a PTC device is included in a circuit and an abnormal current passes through the circuit, the device enters the higher temperature condition and, thereby, switches into the higher resistance condition to decrease the current passing through the circuit to a minimal level and, thus, protect electric elements of the circuit and the baftery/ies. At the minimal level (e.g., about 20% of peak current), the battery can cool off to a "safe" level at which time greater power can be supplied. The partially conducting layer of the PTC device is, for example, a composite of carbon powder and polyolefin plastic. Further description of such devices is unnecessary, as these devices are described and are well known in the art.
Because PTC circuits of different manufacturers operate with different characteristic behaviors, the present invention takes advantage of this feature and provides a process for optimizing the selection of a particular battery to match a particular motor and a particular use.
An examination of the time when the PTC device switches to the higher resistance condition can be used as this indicator for optimizing a particular motor and drive train to a battery. It is desirable to know when the PTC device makes this switch so that, during normal stapler use, the PTC device does not make this change.
Exemplary batteries were loaded with various levels from approximately 3 amps to approximately 8 amps. At the high end, the PTC device changed to the high-resistance state almost immediately, making this current level too high for standard CR123 cells. It was determined that, for between 4 and 6 amps, one manufacturer's cell had PTC
activation sooner than another manufacturer's cell. The longest PTC changeover duration for the second manufacturer was >3 minutes for 4 amps, approximately 2 minutes for 5 amps, and almost 50 seconds for 6 amps. Each of these durations was significantly greater than the 8-second peak load requirement. Accordingly, it was determined that the second manufacturer's cells would be optimal for use at peak amps as compared to the first manufacturer's cells.
Initially, it was surmised that higher amperes with lower or constant voltage would generate higher power out of the power cell(s). Based upon the configuration of 6 cells in series, the peak voltage could be 18 volts with a peak current of only 6 amps. Placing cells in parallel, in theory, should allow a higher peak amperage and a 3x2 configuration (two parallel set of three cells in series) could have a 9 volt peak with up to a 12 amp peak.
Different single cells were investigated and it was confirmed that a relatively low voltage (about 1.5 to 2 volts) and approximately 4 to 6 amperes produces the highest power in Watts. Two six-cell configurations were examined: a 6x1 series connection and a 3x2 parallel connection.
The 3x2 configuration produced the greatest peak amperes of approximately 10 amps. The 6x1 configuration produced about 6 amps peak and the single cell was able to peak at 5-6 amps before the PTC device changed state. This information indicated the state at which any single cell in the series group would be activating its PTC device and, thus, limiting current through the entire group of cells. Thus, the tentative conclusion of yielding peak amps at lower voltage with a 3x2 configuration was maintained.
Three different CR123 battery configurations were tested: 4x1, 6x1, and 3x2, to see how fast the pinion would move the rack (in inches per second ("IFS")) for the 120# and 180# loads and for a given typical gearing. The results of this real world dynamic loading test are shown in the chart of FIG. 31, for both the 120# load:
= the 4x1 battery pack was able to move the load at about 0.6 IFS at 5 approximately 2.5 amps but at approximately 8 volts;
= the 6x1 battery pack was able to move the load at about 0.9 IPS at approximately 2.5 amps but at approximately 13 volts; and = the 3x2 battery pack was able to move the load at about 0.4 TS at approximately 2.5 amps but at approximately 6 volts;
and the 180# load:
= the 4x1 battery pack was able to move the load at about 0.65 IFS at approximately 4 amps but at approximately 7.5 volts;
= the 6x1 battery pack was able to move the load at about 0.9 IFS at approximately 4 amps but at approximately 12 volts; and = the 3x2 battery pack was able to move the load at about 0.4 [PS at approximately 4 amps but at approximately 7 volts.
Clearly, the peak current was limited and this limit was dependent upon the load. This experiment revealed that the motor drew a similar current regardless of the power supply for a given load but that the voltage changed depending upon the battery cell configuration. With respect to either load, the power output was the greatest in the 6x1 configuration and not in the 3x2 configuration, as was expected. From this, it was determined that the total power of the cell pack is driven by voltage and not by current and, therefore, the parallel configuration (3x2) was not the path to take in optimizing the power source.
Traditionally, when designing specifications for a motor, the windings of the motor are matched to the anticipated voltage at which the motor will be run. This matching takes into account the duration of individual cycles and the desired overall life of the product. In a case of an electric stapling device the motor will only be used for very short cycles and for a very short life, traditional matching methods yield results that are below optimal.
Manufacturers of the motors give a voltage rating on a motor that corresponds to the number of turns of the windings. The lower the number of turns, the lower the rated voltage. Within a given size of motor winding, a lower number of turns allows larger wire to be used, such that a lower number of turns results in a lower resistance in the windings, and a higher number of turns results in a higher resistance.
These characteristics limit the maximum current that the motor will draw, which is what creates most of the heat and damage when the motor is overdriven. For the present invention, a desirable configuration will have the lowest winding resistance to draw the most current from the power supply (i.e., battery pack). By running the motor at a voltage much higher than the motor rating, significantly greater power can be drawn from similarly sized motors. This trait was verified with testing of nearly identical careless motors that only varied in winding resistance (and, hence, the number of turns). For example, 12-volt and 6-volt rated motors were run with 6 cells (i.e., at 19.2 volts). The motors rated for 12 volts output peak power of 4 Watts with the battery voltage only falling slightly to 18 volts when drawing 0.7 amps. In comparison, the motors rated for 6 volts output 15 Watts of power with the voltage dropping to 15 volts but drawing 2 amps of current.
Therefore, the lower resistance windings were selected to draw enough power out of the batteries.
It is noted that the motor windings should be balanced to the particular battery pack so that, in a stall condition, the motor does not draw current from the cells sufficient to activate the PTC, which condition would impermissibly delay use of an electric surgical stapler during an operation.
The 6x1 power cell configuration appeared to be more than sufficient to meet the requirements of the electric stapling device. Nonetheless, at this point, the power cell can be further optimized to determine if six cells are necessary to perform the required work. Four cells were, then, tested and it was determined that, under the 120# load, the motor/drive train could not move the rack over the 60 mm span within 3 seconds. Six cells were tested and it was determined that, under the 120# load, the motor/drive train could move the rack over the 60 mm span in 2.1 seconds ¨ much faster than the 3-second requirement. It was further determined that, under the 180# load, the motor/drive train could move the rack over the 60 mm span in less than 2.5 seconds ¨ much quicker than the 8-second requirement. At this point, it is desirable to optimize the power source and mechanical layout to make sure that there is no "runaway"
stapling/cutting; in other words, if the load is significantly less than the required 180# maximum, or even the 120#
maximum, then it would not be desirable to have the rack move too fast.
The gear reduction ratio and the drive system need to be optimized to keep the motor near peak efficiency during the firing stroke. The desired stroke of 60 mm in 3 seconds means a minimum rack velocity of 20 mm/sec (-0.8 inches/second). To reduce the number of variables in the optimization process, a basic reduction of 333:1 is set in the gear box.
This leaves the final reduction to be performed by the gears present between the output shaft 214 of the gear box and the rack 217, which gears include, for example, a bevel gear 215 and the pinion 216 (which drives the rack), a simplified example of which is illustrated in FIG. 32.
These variables can be combined into the number of inches of rack travel with a single revolution of the output shaft 214 of the 333:1 gearbox. If the gearbox output (in rpm) never changed, it would be a simple function to match the inches of rack travel per output shaft revolution ("IPR") to the output rpm to get a desired velocity as follows:
(60 rpm 1 revolution/second (rps); 1 rps @ 0.8 IPR 4 0.8 in/see).
In such an idealized case, if the IPR is plotted against velocity, a straight line would be produced.
Velocity over a fixed distance can be further reduced to Firing Time. Thus, a plot of Firing Time versus IPR would also be a straight line in this idealized case. However, output of the motor (in rpm) and, therefore, of the gearbox, is not fixed because this speed varies with the load. The degree of load determines the amount of power the motor can put out. As the load increases, the rpms decrease and the efficiency changes. Based upon an examination of efficiency with differing loads, it has been determined that efficiency peaks at just over 60%. However, the corresponding voltage and amperes at this efficiency peak .are not the same as at the point of peak power. Power continues to increase as the load increases until the efficiency is falling faster than the power is increasing. As the MR increases, an increase in velocity is expected, but a corresponding increase in IPR lowers the mechanical advantage and, therefore, increases the load.
This increasing load, with the corresponding decrease in efficiency at progressively higher loads, means that a point will exist when greater velocity out of the rack is no longer possible with greater IPR. This behavior is reflected as a deviation from a predicted straight line in the plot of Firing Time (in sec) versus IPR. Experimentation of the system of the present invention reveals that the boundary between unnecessary mechanical advantage and insufficient mechanical advantage occurs at approximately 0.4 IPR.
From this IPR value, it is possible to, now, select the final gear ratio of the bevel gear 215 to be approximately three times greater (3:1) than the sprocket of the output shaft. This ratio translates into an approximate IPR of 0.4.
Now that the bevel gear 215 has been optimized, the battery pack can be reexamined to deten-nine if six cells could be reduced to five or even four cells, which would save cost and considerably decrease the volume needed for the power supply within the handle. A constant load of approximately 120# was used with the optimized motor, drive train, bevel gear, and rack and pinion and it was discovered that use of 4 cells resulted in an almost 5 second time period for moving the rack 60 mm. With 5 cells, the time was reduced to approximately 3.5 seconds. With a 6-cell configuration, the time was 2.5 seconds. Thus, interpolating this curve resulted in a minimum cell configuration of 5.5 cells. Due to the fact that cells only can be supplied in integer amounts, it was discovered that the 6-cell configuration was needed to meet the requirements provided for the electric stapling device.
From this, the minimum power source volume could be calculated as a fixed value, unless different sized cells could be used that provided the same electrical power characteristics. Lithium cells referred as CR2s have similar electrical power characteristics as have CR123s but are smaller. Therefore, using a 6-cell power supply of CR2s reduced the space requirement by more than 17%.
As set forth in detail above, the power source (i.e., batteries), drive train, and motor are optimized for total efficiency to deliver the desired output force within the required window of time for completing the surgical procedure. The efficiency of each kind of power source, drive train, and motor was examined and, thereafter, the type of power source, drive train, and motor was selected based upon this examination to deliver the maximum power over the desired time period. In other words, the maximum-power condition (voltage and current) is examined that can exist for a given period of time without activating the PTC (e.g., approximately 15 seconds). The present invention locates the voltage-current-power value that optimizes the way in which power is extracted from the cells to drive the motor. Even after such optimization, other changes can be made to improve upon the features of the electric stapler 1.
Another kind of power supply can be used and is referred to herein as a "hybrid" cell. In such a configuration, a rechargeable Lithium-ion or Lithium-polymer cell is connected to one or more of the optimized cells mentioned above (or perhaps another primary cell of smaller size but of a similar or higher voltage). In such a configuration, the Li-ion cell would power the stapling/cutting motor because the total energy contained within one CR2 cell is sufficient to recharge the Li ion cell many times, however, the primary cells are limited as to delivery. Li-ion and Li-Polymer cells have very low internal resistance and are capable of very high currents over short durations. To harness this beneficial behavior, a primary cell (e.g., CR123, CR2, or another cell) could take 10 to 30 seconds to charge up the secondary cell, which would form an additional power source for the motor during firing. An alternative embodiment of the Li-ion cell is the use of a capacitor; however, capacitors are volume inefficient. Even so, a super capacitor may be put into the motor powering system; it may be disconnected electrically therefrom until the operator determines that additional power is required. At such a time, the operator would connect the capacitor for an added "boost" of energy.
As mentioned above, if the load on the motor increases past a given point, the efficiency begins to decrease. In such a situation, a multi-ratio transmission can be used to change the delivered power over the desired time period. When the load becomes too great such that efficiency decreases, a multi-ratio transmission can be used to switch the gear ration to return the motor to the higher efficiency point, at which, for example, at least a 180#
force can be supplied.
It is noted, however, that the motor of the present invention needs to operate in both forward and reverse directions. In the latter operating mode, the motor must be able to disengage the stapling/cutting instrument from out of a "jammed" tissue clamping situation.
Thus, it would be beneficial for the reverse gearing to generate more force than the forward gearing.
With significantly varying loads, e.g., from low pounds up to 180 pounds, there is the possibility of the drive assembly being too powerful in the lower end of the load range. Thus, the invention can include a speed governing device. Possible governing devices include dissipative (active) governors and passive governors. One exemplary passive governor is a flywheel, such as the energy storage element 56, 456 disclosed in U.S. Patent Application No.
2005/0277955 to Palmer et al. Another passive governor that can be used is a "fly"
paddlewheel. Such an assembly uses wind resistance to govern speed because it absorbs more force as it spins faster and, therefore, provides a speed governing characteristic when the motor is moving too fast.
Another kind of governor can be a compression spring that the motor compresses slowly to a compressed state.
When actuation is desired, the compressed spring is released, allowing all of the energy to be transferred to the drive in a relatively short amount of time. A further exemplary governor embodiment can include a multi-stage switch having stages that are connected respectively to various sub-sets of the battery cells. When low force is desired, a first switch or first part of a switch can be activated to place only a few of the cells in the power supply circuit. As more power is desired, the user (or an automated computing device) can place successive additional cells into the power supply circuit. For example, in a 6-cell configuration, the first 4 cells can be connected to the power supply circuit with a first position of a switch, the fifth cell can be connected with a second position of the switch, and the sixth cell can be connected with a third position of the switch.
Electric motors and the associated gear box produce a certain amount of noise when used.
5 The stapler of the present invention isolates the motor and/or the motor drive train from the handle to decrease both the acoustic and vibration characteristics and, thereby, the overall noise produced during operation. In a first embodiment, a dampening material is disposed between the handle body and both of motor and the drive train. The material can be foam, such as latex, polyester, plant-based, polyether, polyetherimide, polyimide, polyolefin, polypropylene, phenolic, 10 polyisocyanates, polyurethane, silicone, vinyl, ethylene copolymer, expanded polyethylene, fluoropolymer, or styrofoam. The material can be an elastomer, such as silicone, polyurethane, chloroprene, butyl, polybutadiene, neoprene, natural rubber, or isoprene. The foam can be closed cellular, open cellular, flexible, reticular, or syntactic, for example. The material can be placed at given positions between the handle and motor/gear box or can entirely fill the chamber 15 surrounding the motor/gear box. In a second embodiment, the motor and drive train are isolated within a nested box configuration, sometimes referred to as a "Chinese Box" or "Russian nesting doll." In such a configuration, the dampening material is placed around the motor/gear box and the two are placed within a first box with the gear box shaft protruding therefrom. Then, the first box is mounted within the "second box" ¨ the handle body ¨ and the dampening material is place 20 between the first box and the handle interior.
The electric stapler of the present invention can be used in surgical applications. Most stapling devices are one-time use. They can be disposed after one medical procedure because the cost is relatively low. The electric surgical stapler, however, has a greater cost and it may be desirable to use at least the handle for more than one medical procedure.
Accordingly, 25 sterilization of the handle components after use becomes an issue.
Sterilization before use is also significant. Because the electric stapler includes electronic components that typically do not go through standard sterilization processes (i.e., steam or gamma radiation), the stapler needs to be sterilized by other, possibly more expensive, means such as ethylene-oxide gas. It would be desirable, however, to make the stapler available to gamma radiation sterilization to reduce the 30 cost associated with gas sterilization. It is known that electronics are usable in space, which is an environment where such electronics are exposed to gamma radiation. In such applications, however, the electronics need to work while being exposed. In contrast, the electric stapler does not need to work while being exposed to the gamma sterilization radiation.
When semiconductors are employed, even if the power to the electronics is turned off, gamma radiation will adversely affect the stored memory. These components only need to withstand such radiation and, only after exposure ceases, need to be ready for use. Knowing this, there are various measures that can be taken to gamma-harden the electronic components within the handle. First, instead of use MOSFET memory, for example, fusable link memories can be used. For such memories, once the fuses are programmed (i.e., burnt), the memory becomes permanent and resistant to the gamma sterilization_ Second, the memory can be mask-programmed. If the memory is hard programmed using masks, gamma radiation at the level for medical sterilization will not adversely affect the programming. Third, the sterilization can be performed while the volatile memory is empty and, after sterilization, the memory can be programmed through various measures, for example, a wireless link including infrared, radio, ultrasound, or Bluetooth communication can be used.
Alternatively, or additionally, external electrodes can be contacted in a clean environment and these conductors can program the memory. Finally, a radiopaque shield (made from molybdenum or tungsten, for example) can be provided around the gamma radiation sensitive components to prevent exposure of these components to the potentially damaging radiation.
As set forth herein, characteristics of the battery, drive train, and motor are examined and optimized for an electric stapling application. The particular design (i.e., chemistry and PTC) of a battery will determine the amount of current that can be supplied and/or the amount of power that can be generated over a period of time. It has been determined that standard alkaline cells do not have the ability to generate the high power needed over the short period of time to effect actuation of the electric stapling device. It was also determined that some lithium-manganese dioxide cells also were unable to meet the needs for actuating the stapling device.
Therefore, characteristics of certain lithium-manganese dioxide cell configurations were examined, such as the electrolyte and the positive temperature coefficient device.
It is understood that conventional lithium-manganese dioxide cells (e.g., CR123 and CR2) are designed for loads over a long period of time. For example, SUREFIRE
markets flashlights and such cells and states that the cells will last for from 20 minutes to a few hours (3 to 6) at the maximum lumen output of the flashlight. Load upon the cells(s) during this period of time is not close to the power capacity of the battery(ies) and, therefore, the critical current rate of the battery(ies) is not reached and there is no danger of overheating or explosion. If such use is not continuous, the batteries can last through many cycles (i.e., hundreds) at this same full power output.
Simply put, such batteries are not designed for loads over a period of 10 seconds or less, for example, five seconds, and are also not designed for a small number of uses, for example, ten to fifteen. What the present invention does is to configure the power supply, drive train, and motor to optimize the power supply (i.e., battery) for a small number of uses with each use occurring over a period of less than ten seconds and at a load that is significantly higher than rated.
All of the primary lithium cells that were examined possess a critical current rate defined by the respective PTC device and/or the chemistry and internal construction.
If used above the critical current rate for a period of time, the cells can overheat and, possibly, explode. When exposed to a very high power demand (close to the PTC threshold) with a low number of cycles, the voltage and amperage profiles do not behave the same as in prior art standard uses. It has been found that some cells have PTC devices that prevent generation of power required by the stapler of the present invention, but that other cells are able to generate the desired power (can supply the current an voltage) for powering the electric stapling device. This means that the critical current rate is different depending upon the particular chemistry, construction, and/or PTC of the cell.
The present invention configures the power supply to operate in a range above the critical current rate, referred to herein as the "Super-Critical Current Rate." It is noted within the definition of Super-Critical Current Rate also is an averaging of a modulated current supplied by the power supply that is above the critical current rate. Because the cells cannot last long while supplying power at the Super-Critical Current Rate, the time period of their use is shortened. This shortened time period where the cells are able to operate at the Super-Critical Current Rate is referred to herein as the "Super-Critical Pulse Discharge Period," whereas the entire time when the power supply is activated is referred to as a "Pulse Discharge Period." In other words, the Super-Critical Pulse Discharge Period is a time that is less than or equal to the Pulse Discharge Period, during which time the current rate is greater than the critical current rate of the cells. The Super-Critical Pulse Discharge Period for the present invention is less than about 16 seconds, in other words, in a range of about one-half to fifteen seconds, for example, between two and four seconds and, more particularly, at about three seconds. During the life of the stapling device, the power supply may be subjected to the Super-Critical Current Rate over the Pulse Discharge Period for at least one time and less than twenty times within the time of a clinical procedure, for example, between approximately five and fifteen times, in particular, between ten and fifteen times within a period of five minutes. Therefore, in comparison to the hours of use for standard applications of the power supply, the present invention will have an aggregate use, referred to as the Aggregate Pulse Time, of, at most, approximately 200 to 300 seconds, in particular, approximately 225 seconds. It is noted that, during an activation, the device may not be required to exceed or to always exceed the Super-Critical Current Rate in a given procedure because the load presented to the instrument is dependent upon the specific clinical application (i.e., some tissue is denser than others and increased tissue density will increase toad presented to device).
However, the stapler is designed to be able to exceed the Super-Critical Current Rate for a number of times during the intended use of the surgical procedure. Acting in this Super-Critical Pulse Discharge Period, the device can operate a sufficient amount of times to complete the desired surgical procedure, but not many more because the power supply is asked to perform at an increased current.
When performing in the increased range, the force generated by the device, e.g., the electric stapler 1, is significantly greater than existed in a hand-powered stapler. In fact, the force is so much greater that it could damage the stapler itself. In one exemplary use, the motor and drive assemblies can be operated to the detriment of the knife blade lock-out feature -- the safety that prevents the knife blade 1060 from advancing when there is no staple cartridge or a previously fired staple cartridge in the staple cartridge holder 1030. This feature is illustrated in FIG. 33. As discussed, the knife blade 1060 should be allowed to move distally only when the staple sled 102 is present at the firing-ready position, i.e., when the sled 102 is in the position illustrated in FIG.
33. If the sled 102 is not present in this position, this can mean one of two things, either there is no staple cartridge in the holder 1030 or the sled 102 has already been moved distally ¨ in other words, a partial or full firing has already occurred with the loaded staple cartridge. Thus, the blade 1060 should not be allowed to move, or should be restricted in its movement.
Accordingly, to insure that the sled 102 can prop up the blade 1060 when in a firing state, the sled 102 is provided with a lock-out contact surface 104 and the blade 1060 is provided with a correspondingly shaped contact nose 1069. It is noted at this point that, the lower guide wings 1065 do not rest against a floor 1034 in the cartridge holder 1030 until the blade 1060 has moved distally past an edge 1035.
With such a configuration, if the sled 102 is not present at the distal end of the blade 1060 to prop up the nose 1069, then the lower guide wings 1065 will follow the depression 1037 just proximal of the edge 1035 and, instead of advancing on the floor 1034, will hit the edge 1035 and prevent further forward movement of the blade 1060. To assist with such contact when the sled 102 is not present (referred to as a "lock out"), the staple cartridge 1030 has a plate spring 1090 (attached thereto by at least one rivet 1036) for biasing the blade 1060. With the plate spring 1090 flexed upward and pressing downward against the flange 1067 (at least until the flange 1067 is distal of the distal end of the plate spring 1090), a downwardly directed force is imparted against the blade 1060 to press the wings 1065 down into the depression 1037. Thus, as the blade 1060 advances distally without the sled 102 being present, the wings 1065 follow the lower curve of the depression 1037 and are stopped from further distal movement when the distal edge of the wings 1065 hit the edge 1035.
This safety feature operates as described so long as the force transmitted by the knife blades 1062 to the blade 1060 is not great enough to tear off the lower guide wings1065 from the blade 1060. With the forces able to be generated by the power supply, motor and drive train of the present invention, the blade 1060 can be pushed distally so strongly that the wings 1065 are torn away. If this occurs, there is no way to prevent distal movement of the blade 1060 or the sled 102.
Accordingly, the present invention provides a way to lower the forces able to be imparted upon the wings 1065 prior to their passage past the edge 1035. In other words, the upper limit of force able to be applied to the blade 1060 is reduced in the first part of blade travel (past the edge 1035) and increases after the wings 1065 have cleared the edge 1035 and rest on the floor 1034. More specifically, a first exemplary embodiment of this two-part force generation limiter takes the form of a circuit in which only one or a few of the cells in the power supply are connected to the motor during the first part of the stapling/cutting stroke and, in the second part of the stapling/cutting stroke, most or all of the cells in the power supply are connected to the motor. A first exemplary form of such a circuit is illustrated in FIG. 34. In this first embodiment, when the switch 1100 is in the "A" position, the motor (e.g., stapling motor 210) is only powered with one power cell 602 (of a possible four in this exemplary embodiment). However, when the switch 1100 is in the "B"
position, the motor is powered with all four of the cells 602 of the power supply 600, thereby increasing the amount of force that can be supplied to the blade 1060. Control of the switch 1100 between the A and B positions can occur by positioning a second switch somewhere along the blade control assembly or along the sled 102, the second switch sending a signal to a controller after the wings 1065 have passed the edge 1035. It is noted that this first embodiment of the control circuit is only exemplary and any similarly performing assembly can provide the lock-out protection for the device, see, for example, the second exemplary embodiment illustrated in FIG.
36.
A first exemplary form of a forward and reverse motor control circuit is illustrated in FIG.
5 35. This first exemplary embodiment uses a double-throw, double pole switch 1200. The switch 1200 is normally spring-biased to a center position in which both poles are off. The motor M
illustrated can, for example, represent the stapling motor 210 of the present invention. As can be seen, the power-on switch 1210 must be closed to turn on the device. Of course, this switch is optional. When a forward movement of the motor M is desired, the switch 1200 is placed in the 10 right position as viewed in FIG. 35, in which power is supplied to the motor to run the motor in a first direction, defined as the forward direction here because the "+" of the battery is connected to the "+" of the motor M. In this forward switching position, the motor M can power the blade 1060 in a distal direction. Placement of an appropriate sensor or switch to indicate the forward-most desired position of the blade 1060 or the sled 102 can be used to control a forward travel limit 15 switch 1220 that interrupts power supply to the motor M and prevents further forward travel, at least as long as the switch 1220 remains open. Circuitry can be programmed to never allow this switch 1220 to close and complete the circuit or to only allow resetting of the switch 1220 when a new staple cartridge, for example, is loaded.
When a reverse movement of the motor M is desired, the switch 1200 is placed in the left 20 position as viewed in FIG. 35, in which power is supplied to the motor to run the motor in a second direction, defined as the reverse direction here because the "-" of the battery is connected to the "+" of the motor M. In this reverse switching position, the motor M can power the blade 1060 in a proximal direction. Placement of an appropriate sensor or switch to indicate the rearward-most desired position of the blade 1060 or the sled 102 can be used to control a rearward 25 travel limit switch 1230 that interrupts power supply to the motor M and prevents further rearward travel, at least as long as the switch 1230 remains open. It is noted that other switches (indicated with dotted arrows) can be provided in the circuit to selectively prevent movement in either direction independent of the limit switches 1220, 1230.
It is noted that the motor can power the gear train with a significant amount of force, which 30 translates into a high rotational inertia. As such, when any switch mentioned with respect to FIGS. 34 and 35 is used to turn off the motor, the gears may not just stop.
Instead, the rotational inertia continues to propel, for example, the rack 217 in the direction it was traveling when power to the motor was terminated. Such movement can be disadvantageous for many reasons. By configuring the power supply and motor appropriately, a circuit can be formed to substantially eliminate such post-termination movement, thereby giving the user more control over actuation.
FIG. 36 illustrates an exemplary embodiment where the motor (for example, stapling motor 210) is arrested from further rotation when forward or reverse control is terminated. FIG.
36 also illustrates alternative embodiments of the forward/reverse control and of the multi-stage power supply. The circuit of FIG. 36 has a motor arrest sub-circuit utilizing a short-circuit property of an electrical motor. More specifically, the electrical motor M is placed into a short-circuit so that an electrically generated magnetic field is created in opposition to the permanent magnetic field, thus slowing the still-spinning motor at a rate that substantially prevents inertia-induced over-stroke. To explain how the circuit of FIG. 36 can brake the motor M, an explanation of the forward/reverse switch 1300 is provided. As can be seen, the forward/reverse switch 1300 has three positions, just like the switch 1200 of FIG. 35. When placed in the right position, the motor M is actuated in a forward rotation direction. When placed in the left position, the motor M
is actuated in a rearward rotation direction. When the switch 1300 is not actuated ¨ as shown in FIG. 36¨ the motor M is short circuited. This short circuit is diagrammatically illustrated by the upper portion of the switch 1300. It is noted that the switching processes in a braking switch is desired to take place in a time-delayed manner, which is also referred to as a break-before-make switching configuration. When switching over from operating the motor M to braking the motor M, the double-pole, double throw portion of the forward/reverse switch 1300 is opened before the motor short circuit is effected. Conversely, when switching over from braking the motor M to operating the motor M, the short circuit is opened before the switch 1300 can cause motor actuation. Therefore, in operation, when the user releases the 3-way switch 1300 from either the forward or reverse positions, the motor M is short-circuited and brakes quickly.
Other features of the circuit in FIG. 36 have been explained with regard to FIG. 35. For example, an on/off switch 1210 is provided. Also present is the power lock-out switch 1100 that only powers the motor with one power cell 602' in a given portion of the actuation (which can occur at the beginning or at any other desired part of the stroke) and powers the motor M with all of the power cells 602 (here, for example, six power cells) in another portion of the actuation.
A new feature of the reverse and forward limit switches 1320, 1330 prevents any further forward movement of the motor M after the forward limit switch 1320 is actuated. When this limit is reached, the forward limit switch 1320 is actuated and the switch moves to the second position. In this state, no power can get to the motor for forward movement but power can be delivered to the motor for reverse movement. The forward limit switch can be programmed to toggle or be a one-time use for a given staple cartridge. More specifically, the switch 1320 will remain in the second position until a reset occurs by replacing the staple cartridge with a new one.
Thus, until the replacement occurs, the motor M can only be powered in the reverse direction. If the switch is merely a toggle, then power can be restored for additional further movement only when the movement has retreated the part away from actuating the switch 1320.
The reverse limit switch 1330 can be configured similarly. When the reverse limit is reached, the switch 1330 moves to the second position and stays there until a reset occurs. It is noted that, in this position, the motor M is in a short-circuit, which prevents motor movement in either direction. With such a configuration, the operation of the stapler can be limited to a single stroke up to the forward limit and a single retreat up to the rear limit. When both have occurred, the motor M is disabled until the two switches 1320 are reset.
The foregoing description and accompanying drawings illustrate the principles, preferred embodiments and modes of operation of the invention. More specifically, the optimized power supply, motor, and drive train according to the present invention has been described with respect to a surgical stapler. However, the invention should not be construed as being limited to the particular embodiments discussed above. Additional variations of the embodiments discussed above will be appreciated by those skilled in the art as well as for applications, unrelated to surgical devices, that require an advanced power or current output for short and limited durations with a power cell having a limited power or current output. As is shown and described, when optimized according to the present invention, a limited power supply can produce lifting, pushing, pulling, dragging, retaining, and other kinds of forces sufficient to move a substantial amount of weight, for example, over 82 kg.
The above-described embodiments should be regarded as illustrative rather than restrictive.
Accordingly, it should be appreciated that variations to those embodiments can be made by those skilled in the art without departing from the scope of the invention as defined by the following claims.

Claims (191)

1. An optimal tissue compression surgical device, comprising:
a handle having therein a compression controller adapted to be electrically coupled to a power supply selectively supplying power therefrom; and a surgical end effector connected to said handle and having:
an electrically controlled tissue-compressing device operable to compress tissue disposed therein, said tissue-compressing device being electrically coupled with said compression controller and being powered thereby to selectively control compression of the tissue disposed within said tissue-compressing device; and a mechanical binary-output electrical switch disposed in line with said tissue-compressing device to place a force upon said mechanical binary-output electrical switch proportional to a compressing force directed upon the compressed tissue, said mechanical binary-output electrical switch having:
first and second electrical switching states initiated and changed solely by mechanical movements;
a biasing device retaining said switch in said first switching state with a bias force until a force imparted upon said switch overcomes said bias force to change said switch to said second switching state; and a switching-state-status output communicatively coupled to said compression controller and operable to provide information identifying a current one of said switching states, said compression controller being operable to selectively control compression of the tissue disposed within said tissue-compressing device based upon said information.

2. The device according to claim 1, further comprising:
an entirely self-contained power supply disposed in said handle;
said compression controller being electrically coupled to said power supply to selectively supply power therefrom;
said tissue-compressing device being electrically coupled with said compression controller and said power supply; and said biasing device operable to retain said switch in said first switching state until a force at least as great as said bias force is imparted to said switch to change said switch to said second switching state.

3. The device according to claim 1, wherein:
said end effector has a tissue surgery device operable to carry out a surgical procedure on the tissue compressed by said tissue-compressing device;
a procedure control switch is disposed at said handle and is coupled to said tissue surgery device to selectively commence and halt said surgical procedure, said procedure control switch having a commence position; and said tissue surgery device is communicatively coupled with said compression controller and is operable to carry out said surgical procedure on the compressed tissue:
only when said procedure control switch is in said commence position; and only after force imparted to said electrical switch is sufficient to switch from said first switching state to said second switching state and, thereby, change said information at said switching-state-status output.

4. The device according to claim 1, wherein:
said end effector has a tissue surgery device operable to carry out a surgical procedure on the tissue compressed by said tissue-compressing device;
a procedure control switch is disposed at said handle and is coupled to said tissue surgery device to selectively commence and halt said surgical procedure, said procedure control switch having a commence position; and said tissue surgery device is communicatively coupled with said compression controller and is operable to carry out said surgical procedure on the compressed tissue:
only when said procedure control switch is in said commence position; and only while the force imparted to said electrical switch is sufficient to switch from said first switching state to said second switching state and, thereby, change said information at said switching-state-status output.

5. The device according to claim 1, further comprising a compression-start switch at said handle, said compression-start switch being communicatively coupled with said compression controller to selectively commence and halt compression of the tissue by said tissue-compressing device.

6. The device according to claim 1, wherein said biasing device is adjustable and applies said bias force over a range of bias force values.

7. The device according to claim 1, wherein:
said surgical end effector is a surgical stapling and cutting end effector having:
a pair of opposing stapling surfaces, at least one of said stapling surfaces being movable with respect to the other of said stapling surfaces along a compression axis to compress tissue therebetween and to staple the tissue compressed therebetween, said movable surface forming at least a first part of said tissue-compression device; and a knife assembly disposed to cut the tissue compressed between said stapling surfaces;
said compression controller is a stapler-closing controller to be electrically coupled with the power supply and selectively supply power therefrom; and an electrically-powered stapler-closing device:
is mechanically coupled to said movable stapling surface to displace said movable surface when powered; and forms at least a second part of said tissue-compressing device; and said electrical switch is disposed in line with said stapler-closing device along said compression axis.

8. The device according to claim 7, wherein:
said switch has a switch actuation gap;
said compression axis spans said gap; and a change of said switching states is dependent upon a force placed along said compression axis.

9. The device according to claim 8, wherein said switch actuation gap is between approximately 25 micrometers and 200 micrometers in width.

10. An optimal tissue compression surgical endocutter, comprising:
a handle having therein a stapler-closing controller adapted to be electrically coupled with a power supply selectively supplying power therefrom; and a surgical stapling and cutting end effector connected to said handle and having:
a pair of opposing stapling surfaces, at least one of said surfaces being movable with respect to the other of said stapling surfaces along a compression axis to compress tissue therebetween and to staple the tissue compressed therebetween;
an electrically-powered stapler-closing device electrically coupled with said stapler-closing controller and being powered thereby to selectively control compression of the tissue disposed between said stapling surfaces, said stapler-closing device being mechanically coupled to said movable stapling surface to displace said movable surface when powered;
a knife assembly disposed to cut the tissue compressed between said stapling surfaces; and a mechanical binary-output electrical switch disposed in line with said stapler-closing device along said compression axis to place a force upon said switch proportional to a compressing force directed upon the compressed tissue, said switch having:
first and second electrical switching states initiated and changed solely by mechanical movements;
a biasing device retaining said switch in said first switching state with a bias force until a force imparted upon said switch overcomes said bias force to change said switch to said second switching state; and a switching-state-status output communicatively coupled to said stapler-closing controller and operable to provide information identifying a current one of said switching states, said stapler-closing controller being operable to selectively control compression of the tissue disposed within said stapler-closing device based upon said information.

11. The endocutter according to claim 10, further comprising:
an entirely self-contained power supply disposed in said handle;
said stapler-closing controller being electrically coupled to said power supply to selectively supply power therefrom;
said stapler-closing device being electrically coupled with said stapler-closing controller and said power supply; and said biasing device retaining said switch in said first switching state with said bias force until a force at least as great as the force imposed by said biasing device is imparted to said switch to change said switch to said second switching state.

12. The endocutter according to claim 10, wherein:
said end effector has a tissue surgery device operable to surgically staple and cut the tissue compressed by said stapling surfaces;
a procedure control switch is disposed at said handle and is coupled to said tissue surgery device to selectively commence and halt said surgical stapling and cutting with said tissue surgery device, said procedure control switch having a commence position; and said tissue surgery device is communicatively coupled with said stapler-closing controller and is operable to carry out said surgical stapling and cutting on the compressed tissue:

only when said procedure control switch in said commence position; and only after the force imparted to said electrical switch is sufficient to switch from said first switching state to said second switching state and, thereby, change said information at said switching-state-status output.

13. The endocutter according to claim 10, wherein:
said end effector has a tissue-surgery device operable to surgically staple and cut the tissue compressed by said stapling surfaces;
a procedure control switch is disposed at said handle and is coupled to said tissue surgery device to selectively commence and halt said surgical stapling and cutting with said tissue surgery device, said procedure control switch having a commence position; and said tissue surgery device is communicatively coupled with said stapler-closing controller and is operable to carry out said surgical stapling and cutting on the compressed tissue:
only when said procedure control switch in said commence position; and only while the force imparted to said electrical switch is sufficient to switch from said first switching state to said second switching state and, thereby, change said information at said switching-state-status output.

14. The endocutter according to claim 10, further comprising a compression-start switch at said handle, said compression-start switch being communicatively coupled with said stapler-closing controller to selectively commence and halt compression of the tissue by said stapler-closing device.

15. The endocutter according to claim 10, wherein said biasing device is adjustable and applies said bias force over a range of bias force values.

16. The endocutter according to claim 10, further comprising an indicator communicatively coupled to said switching-state-status output and operable to inform a user when said switching state is changed.

17. The endocutter according to claim 10, wherein:
said switch has a switch actuation gap of between approximately 25 micrometers and 200 micrometers in width and said compression axis spans said gap; and a change of said switching states is dependent upon a force placed along said compression axis.

18. An optimal tissue compression surgical endocutter, comprising:
a handle having therein:
an electrically-powered tissue compression actuator; and an electrically-powered tissue stapling/cutting actuator; and a surgical stapling and cutting end effector connected to said handle and having:
a tissue-compression device operatively coupled to said compression actuator and having surfaces between which tissue to be surgically operated upon is compressed;
a stapler/cutter operatively coupled to said stapling/cutting actuator; and a mechanical binary-output electrical optimal tissue compression switch:

in line with said tissue-compression device;
having first and second electrical switching states initiated and changed solely by mechanical movements;
operatively coupled to said tissue compression actuator and to said stapling/cutting actuator; and operable:
to control said tissue compression actuator; and to control said tissue stapling/cutting actuator and, thereby, said stapler/cutter dependent upon a given tissue compression existing at said tissue-compression device.

19. The endocutter according to claim 18, wherein said switch comprises:
an entirely self-contained power supply disposed in said handle and electrically coupled to said tissue compression actuator and said stapling/cutting actuator to selectively supply power thereto, and a biasing device retaining said switch in said first switching state until a force at least as great as the force imposed by said biasing device is imparted to said switch to change said switch to said second switching state.

20. The endocutter according to claim 18, wherein said optimal tissue compression switch is operable to control said compression actuator to achieve a predetermined optimal tissue compression of tissue within said tissue-compression device.

21. The endocutter according to claim 18, wherein said optimal tissue compression switch is operable to control said compression actuator to maintain a predetermined optimal tissue compression of tissue within said tissue-compression device.

22. The endocutter according to claim 18, wherein said optimal tissue compression switch is operable to indicate to a user that compressed tissue is compressed with a force substantially equal to a pre-set force value.

23. The endocutter according to claim 18, wherein said optimal tissue compression switch is operable to control said stapling/cutting actuator by permitting actuation thereof only after a predetermined optimal tissue compression of tissue exists within said tissue-compression device.

24. The endocutter according to claim 18, wherein said optimal tissue compression switch is operable to control said stapling/cutting actuator by permitting actuation thereof only while a predetermined optimal tissue compression of tissue exists within said tissue-compression device.

25. A method of configuring a surgical instrument having a surgical tissue-compressing device including a pair of opposing compression surfaces with a tissue compression-measuring device, the method comprising:
providing a mechanical binary-output electrical switch having open and closed electrical switching states initiated and changed solely by mechanical movements;
mechanically coupling the switch with an adjustable biasing device retaining the switch in one of the switching states until a force at least as great as a force imposed by the biasing device is imparted to the switch;
disposing the switch in line with the surgical tissue-compressing device to cause a proportional amount of force that is placed upon compressed tissue disposed between the opposing compression surfaces to be placed upon the switch; and setting the biasing device to an amount of force that is proportional to an optimal tissue compression force of the compressed tissue when disposed between the opposing compression surfaces.

26. The method according to claim 25, which further comprises disposing the switch to cause substantially the same force that is placed upon the compressed tissue disposed between the opposing compression surfaces to be placed upon the switch.

27. The method according to claim 26, wherein setting the biasing device to an amount of force that is proportional to the optimal tissue compression force of the compressed tissue when disposed between the opposing compression surfaces causes a change of the switching state when a compression force placed on tissue by the opposing compression surfaces of the tissue-compressing device is at least as great as the optimal tissue compression force.

28. The method according to claim 25, which further comprises providing an indicator operable to indicate when the switching state is changed.

29. The method according to claim 25, which further comprises providing the switch with a switch actuation gap that is between approximately 25 micrometers and micrometers in width.

30. The method according to claim 29, which further comprises orienting the switch actuation gap to span along a compression axis of the tissue-compressing device and cause a change of the switching state dependent upon a force expanding along the compression axis.

31. A method of configuring a surgical instrument having a surgical tissue-compressing device including a pair of opposing compression surfaces with an adjustable tissue compression-measuring device, the method comprising:

providing a mechanical binary-output electrical switch having open and closed electrical switching states initiated and changed solely by mechanical movements;
mechanically coupling the switch with an adjustable biasing device retaining the switch in one of the switching states until a force at least as great as a force imposed by the biasing device is imparted to the switch;
disposing the switch in line with the surgical tissue-compressing device to cause a proportional amount of force that is placed upon compressed tissue disposed between the opposing compression surfaces to be placed upon the switch; and setting the biasing device to an amount of force that is proportional to an optimal tissue compression force of the compressed tissue when disposed between the opposing compression surfaces to cause a change of the switching state to occur when the switch experiences a force at least as great as the force imposed by the biasing device.

32. The method according to claim 31, which further comprises providing an indicator operable to indicate when the switching state is changed.

33. The method according to claim 31, which further comprises providing the switch with a switch actuation gap that is between approximately 25 micrometers and micrometers in width.

34. The method according to claim 33, which further comprises orienting the switch actuation gap to span along a compression axis of the tissue-compressing device and cause a change of the switching state dependent upon a force expanding along the compression axis.

35. A method for effecting a tissue-compressing surgical procedure at a user-selected tissue compression force, the method comprising:

providing a mechanical binary-output electrical switch having open and closed electrical switching states initiated and changed solely by mechanical movements;
mechanically coupling the switch with an adjustable biasing device retaining the switch in one of the switching states until a force at least as great as a force imposed by the biasing device is imparted to the switch;
disposing the switch in line with a surgical tissue-compressing device including a pair of opposing compression surfaces to cause a proportional amount of force that is placed upon compressed tissue disposed between the opposing compression surfaces to be placed upon the switch;
setting the biasing device to an amount of force that is proportional to an optimal tissue compression force of the compressed tissue when disposed between the opposing compression surfaces;
compressing tissue between the opposing compression surfaces of the tissue-compressing device until a force imparted on the switch is at least as great as the optimal tissue compression force and, at such time, changing the switching state; and after changing the switching state, effecting a surgical procedure on the compressed tissue.

36. The method according to claim 35, which further comprises providing an indicator operable to indicate w hen the switching state is changed.

37. The method according to claim 35, which further comprises providing the switch with a switch actuation gap that is between approximately 25 micrometers and micrometers in width.

38. The method according to claim 37, which further comprises orienting the switch actuation gap to span along a compression axis of the tissue-compressing device and cause a change of the switching state dependent upon a force expanding along the compression axis.

39. The method according to claim 35, which further comprises:
providing the tissue-compressing device as an electrically powered surgical endocutter having an end effector with jaws, a knife assembly for cutting tissue compressed between the jaws, and a stapling assembly for stapling the tissue compressed between the jaws; and effecting the surgical procedure by electrically powering the knife and stapling assemblies at the compressed tissue only after the switching state is changed.

40. A method for effecting a tissue-compressing surgical procedure at a user-selected tissue compression force, which comprises:
providing a mechanical binary-output electrical switch having open and closed electrical switching states initiated and changed solely by mechanical movements;
mechanically coupling the switch with an adjustable biasing device retaining the switch in one of the switching states until a force at least as great as a force imposed by the biasing device is imparted to the switch;
disposing the switch in line with an electrically controlled surgical tissue-compressing device including a pair of opposing compression surfaces to cause a proportional amount of force that is placed upon compressed tissue disposed between the opposing compression surfaces to be placed upon the switch, the tissue-compressing device having an electrically operated tissue-compressing assembly and a feedback controller communicatively connected to the tissue-compressing assembly;
setting the biasing device to an optimal tissue compression force;

electrically connecting the switch to the feedback controller; and compressing tissue between the opposing compression surfaces of the tissue-compressing device until a force imparted on the switch is at least as great as the optimal tissue compression force and, at such time, changing the switching state, which state change communicates to the feedback controller that tissue is being compressed with the optimal tissue compression force.

41. The method according to claim 40, which further comprises permitting a surgical procedure to be carried out on the compressed tissue only after the feedback controller has received a state change signal from the switch.

42. The method according to claim 40, which further comprises permitting a surgical procedure to be carried out on the compressed tissue only while the feedback controller is receiving a state change signal from the switch.

43. The method according to claim 41, which further comprises communicatively connecting the tissue-compressing device to the feedback controller and operating the tissue-compressing device dependent upon a signal from the feedback controller to maintain the optimal tissue compression force on the tissue.

44. The method according to claim 40, which further comprises connecting an indicator to the feedback controller to indicate when the switching state is changed, the indicator being one of a tactile, an audible, and a visual indicator.

45. The method according to claim 40, which further comprises providing the switch with a switch actuation gap that is between approximately 25 micrometers and micrometers in width.

46. The method according to claim 45, which further comprises orienting the switch actuation gap to span along a compression axis of the tissue-compressing device and cause a change of the switching state dependent upon a force expanding along the compression axis.

47. The method according to claim 41, which further comprises:
providing the tissue-compressing device as an electrically powered surgical endocutter having an end effector with jaws, a knife assembly for cutting tissue compressed between the jaws, and a stapling assembly for stapling cut tissue compressed between the jaws; and operating the feedback controller to permit electrically powered cutting and stapling of the compressed tissue only after the feedback controller has received the state change signal from the switch.

48. The method according to claim 42, which further comprises:
providing the tissue-compressing device as an electrically powered surgical endocutter having an end effector with jaws, a knife assembly for cutting tissue compressed between the jaws, and a stapling assembly for stapling cut tissue compressed between the jaws; and operating the feedback controller to permit electrically powered cutting and stapling of the compressed tissue only while the feedback controller is receiving the state change signal from the switch.

49. A method for effecting a tissue compressing, cutting, and stapling surgical procedure at a user-selected tissue compression force, which comprises:
providing a mechanical binary-output OTC electrical switch having OTC-off and OTC-reached electrical states initiated and changed solely by mechanical movements;

disposing the switch in line with an electrically controlled surgical endocutter to cause a force that is proportional to a force that is placed upon compressed tissue within jaws thereof to be placed upon the switch;
mechanically coupling the switch with an adjustable biasing device that is set to an amount of force that is proportional to an optimal tissue compression force of the compressed tissue within the jaws and retains the switch in the OTC-off switching state until a force at least as great as the optimal tissue compression force is imparted to the switch; and permitting a surgical cutting and stapling procedure to be carried out on the tissue compressed within the jaws only after the switch changes to the OTC-reached state.

50. A method of configuring a surgical instrument having a surgical tissue-compressing device including opposing compression surfaces with a tissue-compression-measuring mechanism, the method comprising:
providing a switching element having first and second switching states changed solely by mechanical movements;
mechanically coupling the switching element with a biasing element retaining the switching element in one of the first and second switching states until a pre-determined force is imparted to the switching element, the pre-determined force being an amount of force proportional to an optimal tissue compression force of compressed tissue disposed between the opposing compression surfaces; and positioning the switching element in line with the surgical tissue-compressing device to cause the pre-determined force, proportional to a force placed upon compressed tissue disposed between the opposing compression surfaces, to be placed upon the switching element.

51. The method according to claim 50, wherein the switching element is a mechanical binary-output electrical switch.

52. The method according to claim 51, wherein the first switching state is an open electrical state and the second switching state is a closed electrical state.

53. The method according to claim 50, wherein the biasing element is adjustable.

54. The method according to claim 53, further comprising setting the pre-determined force of the biasing element to an amount proportional to the optimal tissue compression force of the compressed tissue.

55. The method according to claim 50, further comprising positioning the switching element to cause substantially the same force placed upon the compressed tissue disposed between the opposing compression surfaces to be placed upon the switching element.

56. The method according to claim 54, wherein setting of the pre-determined force to an amount proportional to the optimal tissue compression force of the compressed tissue causes a change of the switching state when a compression force placed on tissue by the opposing compression surfaces of the tissue-compressing device is at least as great as the optimal tissue compression force.

57. The method according to claim 50, further comprising:
providing the switching element with an actuation gap; and orienting the actuation gap to span along a compression axis of the tissue-compressing device and cause a change of the switching state dependent upon a force expanding along the compression axis.

58. The method according to claim 50, wherein the surgical tissue-compressing device comprises an end effector with two opposing jaws operable to compress tissue disposed therebetween.

59. A method for configuring a surgical instrument having a surgical tissue-compressing device including opposing compression surfaces with a tissue compression-measuring mechanism, the method comprising:
providing a switching element having first and second switching states changed solely by mechanical movements;
mechanically coupling the switching element with a biasing element imparting a pre-determined force on the switching element to retain the switching element in one of the first and second switching states until a switching force at least as great as a force imposed by the biasing element is imparted to the switching element and causes a change of the switching state to occur, the switching force being an amount of force proportional to an optimal tissue compression force of the compressed tissue disposed between the opposing compression surfaces; and positioning the switching element in line with the surgical tissue-compressing device to cause an amount of force, proportional to the force placed upon compressed tissue disposed between the opposing compression surfaces, to be placed upon the switching element.

60. The method according to claim 59, wherein the switching element is a mechanical binary-output electrical switch.

61. The method according to claim 60, wherein the first switching state is an open electrical state and the second switching state is a closed electrical state.

62. The method according to claim 59, wherein the biasing element is adjustable.

63. The method according to claim 62, further comprising setting the switching force of the biasing element to an amount proportional to the optimal tissue compression force of the compressed tissue.

64. The method according to claim 59, further comprising positioning the switching element to cause substantially the same force placed upon the compressed tissue disposed between the opposing compression surfaces to be placed upon the switching element.

65. The method according to claim 63, wherein setting of the switching force to an amount proportional to the optimal tissue compression force of the compressed tissue causes a change of the switching state when a compression force placed on tissue by the opposing compression surfaces of the tissue-compressing device is at least as great as the optimal tissue compression force.

66. The method according to claim 59, further comprising:
providing the switching element with an actuation gap; and orienting the actuation gap to span along a compression axis of the tissue-compressing device and cause a change of the switching state dependent upon a force expanding along the compression axis.

67. The method according to claim 59, wherein the surgical tissue-compressing device comprises an end effector with two opposing jaws operable to compress tissue disposed therebetween.

68. A surgical device, comprising:
a tissue compression device having a pair of opposing compression surfaces;

a mechanical binary-output electrical switch having open and closed electrical switching states initiated and changed solely by mechanical movements; and an adjustable biasing device mechanically coupled to the switch and retaining the switch in one of the switching states until a force at least as great as a force imposed by the biasing device is imparted to the switch, wherein:
the switch is disposed in line with the tissue compression device to cause a proportional amount of force that is placed upon compressed tissue disposed between the opposing compression surfaces to be placed upon the switch; and the biasing device is set to an amount of force that is proportional to an optimal tissue compression force of the compressed tissue when disposed between the opposing compression surfaces.

69. The surgical device according to claim 68, wherein the switch is disposed to cause substantially the same force that is placed upon the compressed tissue disposed between the opposing compression surfaces to be placed upon the switch.

70. The surgical device according to claim 69, wherein setting the biasing device to an amount of force that is proportional to the optimal tissue compression force of the compressed tissue when disposed between the opposing compression surfaces causes a change of the switching state when a compression force placed on tissue by the opposing compression surfaces is at least as great as the optimal tissue compression force.

71. The surgical device according to claim 68, further comprising an indicator operable to indicate a change in the switching state.

72. The surgical device according to claim 68, wherein the switch further comprises a switch actuation gap that is between approximately 25 micrometers and 200 micrometers in width.

73. The surgical device according to claim 72, wherein the switch actuation gap is oriented to span along a compression axis of the tissue compression device and cause a change of the switching state dependent upon a force expanding along the compression axis.

74. The surgical device according to claim 68, wherein:
the tissue compression device is an electrically powered surgical endocutter having an end effector with jaws, a knife assembly for cutting tissue compressed between the jaws, and a stapling assembly for stapling the tissue compressed between the jaws;
and the knife and stapling assemblies are electrically powered only after the switching state is changed.

75. A surgical device, comprising:
an adjustable tissue compression device having a pair of opposing compression surfaces;
a mechanical binary-output electrical switch having open and closed electrical switching states initiated and changed solely by mechanical movements; and an adjustable biasing device retaining the switch in one of the switching states until a force at least as great as a force imposed by the biasing device is imparted to the switch, wherein:
the switch is disposed in line with the tissue compression device to cause a proportional amount of force that is placed upon compressed tissue disposed between the opposing compression surfaces to be placed upon the switch; and the biasing device is set to an amount of force that is proportional to an optimal tissue compression force of the compressed tissue when disposed between the opposing compression surfaces to cause a change of the switching state to occur when the switch experiences a force at least as great as the force imposed by the biasing device.

76. The surgical device according to claim 75, further comprising an indicator operable to indicate a change in the switching state.

77. The surgical device according to claim 75, wherein the switch further comprises a switch actuation gap that is between approximately 25 micrometers and 200 micrometers in width.

78. The surgical device according to claim 77, wherein the switch actuation gap is oriented to span along a compression axis of the tissue compression device and cause a change of the switching state dependent upon a force expanding along the compression axis.

79. A surgical device operable to carry out a surgical procedure, comprising:
an electrically controlled surgical tissue compression device comprising an electrically operated tissue compression assembly having a pair of opposing compression surfaces;
a feedback controller communicatively coupled to the tissue compression assembly;
a mechanical binary-output electrical switch electrically connected to the feedback controller and having open and closed electrical switching states initiated and changed solely by mechanical movements; and an adjustable biasing device mechanically coupled to the switch and retaining the switch in one of the switching states until a force at least as great as a force imposed by the biasing device is imparted to the switch, wherein:

the switch is disposed in line with the tissue compression device to cause a proportional amount of force that is placed upon compressed tissue disposed between the opposing compression surfaces to be placed upon the switch;
the biasing device is set to an optimal tissue compression force; and tissue is compressed between the opposing compression surfaces of the tissue compression device until a force imparted on the switch is at least as great as the optimal tissue compression force and, at such time, a state change occurs and communicates to the feedback controller that tissue is being compressed with the optimal tissue compression force.

80. The surgical device according to claim 79, wherein a surgical procedure is permitted to be carried out on the compressed tissue only after the feedback controller has received a state change signal from the switch.

81. The surgical device according to claim 79, wherein a surgical procedure is permitted to be carried out on the compressed tissue only while the feedback controller is receiving a state change signal from the switch.

82. The surgical device according to claim 80, wherein the tissue compression device operates dependent upon a signal from the feedback controller to maintain the optimal tissue compression force on the tissue.

83. The surgical device according to claim 79, further comprising an indicator connected to the feedback controller and operable to indicate when the switching state is changed, the indicator being one of a tactile, an audible, and a visual indicator.

84. The surgical device according to claim 79, wherein the switch further comprises a switch actuation gap that is between approximately 25 micrometers and 200 micrometers in width.

85. The surgical device according to claim 84, wherein the switch actuation gap is oriented to span along a compression axis of the tissue compression device and cause a change of the switching state dependent upon a force expanding along the compression axis.

86. The surgical device according to claim 80, wherein:
the tissue compression device is an electrically powered surgical endocutter having an end effector with jaws, a knife assembly for cutting tissue compressed between the jaws, and a stapling assembly for stapling the tissue compressed between the jaws;
and electrically powered cutting and stapling of the compressed tissue is permitted only after the feedback controller has received the state change signal from the switch.

87. The surgical device according to claim 81, wherein:
the tissue compression device is an electrically powered surgical endocutter having an end effector with jaws, a knife assembly for cutting tissue compressed between the jaws, and a stapling assembly for stapling the tissue compressed between the jaws;
and electrically powered cutting and stapling of the compressed tissue is permitted only while the feedback controller is receiving the state change signal from the switch.

88. A surgical device, comprising:
an electrically controlled surgical endocutter operable to compress tissue between jaws thereof and to carry out a surgical procedure on the compressed tissue;
a mechanical binary-output OTC electrical switch having OTC-off and OTC-reached electrical states initiated and changed solely by mechanical movements;
an adjustable biasing device mechanically coupled to the switch, wherein:

the switch is disposed in line with the endocutter to cause a force that is proportional to a force that is placed upon tissue compressed between the jaws to be placed upon the switch;
the biasing device is set to an amount of force that is proportional to an optimal tissue compression force of the tissue compressed between the jaws and retains the switch in the OTC-off switching state until a force at least as great as the optimal tissue compression force is imparted to the switch; and a surgical procedure is permitted to be carried out on the compressed tissue only after the switch changes to the OTC-reached state.

89. An electrically powered surgical instrument, comprising:
a surgical end effector having at least one actuation assembly to effect a surgical procedure when actuated;
a handle mechanically coupled with the end effector and having a shell;
an electric motor disposed within the shell and having:
power terminals at which the motor can be supplied with power; and a drive train operatively coupled to the at least one actuation assembly to actuate the at least one actuation assembly when the motor is supplied with power;
a power supply switch at the handle that selectively controls a supply of power to the motor, the power supply switch having:
a break-before-make switching configuration;

a power-supplying state in which power is supplied to the motor; and a power-removed state in which power is not supplied to the motor; and a post-termination braking circuit having the power supply switch as a component thereof, the post-termination braking circuit electrically short-circuiting the power terminals of the motor with the power-removed state of the power supply switch.

90. The instrument according to claim 89, further comprising a power supply within the shell and electrically connected to the motor through at least one of the power supply switch and the post-termination braking circuit.

91. The instrument according to claim 90, wherein the power supply is a removable battery pack.

92. The instrument according to claim 89, wherein the power supply switch is a three-position switch including:
a forward position in which the three-position switch is in the power-supplying state and is configured to cause the motor to rotate in a forward direction;
a reverse position in which the three-position switch is in the power-supplying state and is configured to cause the motor to rotate in a reverse direction; and an off position in which the three-position switch is in the power-removed state and the motor is caused to prevent rotation at the motor.

93. The instrument according to claim 89, wherein:
the drive train has a rotational inertia when operating;
the motor has:

a rotational inertia when spinning; and a permanent magnetic field; and the post-termination braking circuit is operable to create an electrically-generated magnetic field in opposition to the permanent magnetic field with the rotational inertia of at least one of the drive train and the motor when short-circuiting the power terminals.

94. The instrument according to claim 89, wherein the power supply switch is a double-pole, double-throw switch.

95. The instrument according to claim 89, wherein the end effector, handle, motor, power supply switch, and braking circuit are all operable with only a single hand.

96. An electrically powered surgical instrument, comprising:
a surgical end effector having at least one actuation assembly to effect a surgical procedure when actuated;
a handle mechanically coupled with the end effector and having a shell;
an electric motor disposed within the shell and having:
power terminals at which the motor is supplied with power; and a drive train operatively coupled to the at least one actuation assembly to actuate the at least one actuation assembly when the motor is supplied with power;
a power supply switch at the handle that selectively controls a supply of power to the motor, the power supply switch having:

a break-before-make switching configuration;
a power-supplying state in which power is supplied to the motor; and a power-removed state in which power is not supplied to the motor; and a post-termination braking circuit having the power supply switch as a component thereof, the post-termination braking circuit electrically short-circuiting the power terminals of the motor with the power-removed state of the power supply switch.

97. A method for post-termination braking of an electrical motor in an electrically powered surgical instrument, which comprises:
coupling a surgical end effector to a handle having a shell, the end effector having at least one actuation assembly to effect a surgical procedure;
mechanically coupling a drive train of an electric motor to the actuation assembly, the motor having a permanent magnetic field, the motor and drive train being disposed within the shell, and at least one of the motor, the drive train, and the actuation assembly having an inertia-induced over-stroke characteristic after powered operation;
actuating the actuation assembly by selectively supplying the motor with power with a break-before-make power supply switch of a post-termination braking circuit, the break-before-make power supply switch having an off state that ceases supply of power to the motor; and upon ceasing supply of power to the motor, short-circuiting power terminals of the still-spinning motor with the off state of the power supply switch to create an electrically generated magnetic field in opposition to the permanent magnetic field.

98. The method according to claim 97, further comprising counteracting the inertia-induced over-stroke of at least one of the motor, the drive train, and the actuation assembly with the short-circuit.

99. The method according to claim 97, further comprising carrying out the short-circuiting step to slow the still-spinning motor at a rate that substantially eliminates the inertia-induced over-stroke of at least one of the motor, the drive train, and the actuation assembly.

100. The method according to claim 97, further comprising providing a power supply within the shell and electrically connecting the power supply to the motor.

101. The method according to claim 100, wherein the power supply is a removable battery pack.

102. The method according to claim 97, further comprising:
providing a power supply within the shell and electrically connecting the power supply to the motor; and carrying out the short-circuiting step without short-circuiting the power supply.

103. The method according to claim 100, further comprising carrying out the short-circuiting step without short-circuiting the power supply.

104. The instrument according to claim 97, wherein the break-before-make power supply switch is a double-pole, double throw switch.

105. A surgical instrument, comprising:
a surgical end effector having at least one actuation assembly to effect a surgical procedure when actuated;

a handle mechanically coupled with the end effector and having a shell;
an electric motor disposed within the shell and having:
motor terminals; and a drive train operatively coupled to the at least one actuation assembly to actuate the at least one actuation assembly when the motor is supplied with power;
a power supply having power terminals; and a selective switching connection disposed within the shell and having a break-before-make switch with three positions including a forward position, a reverse position, and an off position, the selective switching connection:
in the forward position, electrically connecting the power terminals to the motor terminals to power the motor in a forward direction;
in the reverse position, electrically connecting the power terminals to the motor terminals to power the motor in a reverse direction; and in the off position, electrically separating at least one of the power terminals from the motor terminals.

106. The instrument according to claim 105, wherein:
the power supply is a removable battery pack and has two power terminals; and the switch of the selective switching connection is a double-pole/double-throw, break-before-make switch with three positions including the forward position, the reverse position, and the off position, and:

in the forward position, electrically connects the two power terminals to the two motor terminals to power the motor in a forward direction;
in the reverse position, electrically connects the two power terminals to the two motor terminals to power the motor in a reverse direction; and in the off position, electrically separates at least one of the two power terminals from the two motor terminals.

107. The instrument according to claim 105, wherein the end effector, handle, motor, and selective switching connection are all operable with only a single hand.

108. The instrument according to claim 105, wherein the end effector is a surgical stapling endocutter.

109. The instrument according to claim 105, w herein:
the motor has a permanent magnetic field; and at least one of the motor, the drive train, and the actuation assembly has an inertia-induced over-stroke characteristic after powered operation.

110. The instrument according to claim 109, further comprising a post-termination braking circuit having the selective switching connection as a component thereof, the post-termination braking circuit electrically short-circuiting the motor terminals with the off position of the switch.

111. The instrument according to claim 110, wherein the inertia-induced over-stroke of at least one of the motor, the drive train, and the actuation assembly is counteracted with the short-circuit.

112. The instrument according to claim 110, wherein the short-circuit slows the still-spinning motor at a rate that substantially eliminates the inertia-induced over-stroke of at least one of the motor, the drive train, and the actuation assembly.

113. The instrument according to claim 105, wherein:
the drive train has a rotational inertia when operating; and the motor has:
a rotational inertia when spinning; and a permanent magnetic field.

114. The instrument according to claim 113, further comprising a post-termination braking circuit having the selective switching connection as a component thereof, the post-termination braking circuit operable to create an electrically-generated magnetic field in opposition to the permanent magnetic field with the rotational inertia of at least one of the drive train and the motor when short-circuiting the motor terminals with the off position of the switch.

115. A surgical instrument, comprising:
a surgical end effector having at least one actuation assembly to effect a surgical procedure when actuated;
a handle mechanically coupled with the end effector and having a shell;
an electric motor disposed within the shell and having:
motor terminals; and a drive train operatively coupled to the at least one actuation assembly to actuate the at least one actuation assembly when the motor is supplied with power;
a power supply having power terminals; and a post-termination braking circuit:
having a selective switching connection disposed within the shell and having a break-before-make switch with three positions including a forward position, a reverse position, and an off position, the selective switching connection:
in the forward position, electrically connecting the power terminals to the motor terminals to power the motor in a forward direction;
in the reverse position, electrically connecting the power terminals to the motor terminals to power the motor in a reverse direction; and in the off position, electrically separating at least one of the power terminals from the motor terminals; and electrically short-circuiting the motor terminals with the off position of the switch.

116. The instrument according to claim 139, wherein:
the power supply is a removable battery pack and has two power terminals; and the switch of the selective switching connection is a double-pole/double-throw, break-before-make switch with three positions including the forward position, the reverse position, and the off position, and:

in the forward position, electrically connects the two power terminals to the two motor terminals to power the motor in a forward direction;
in the reverse position, electrically connects the two power terminals to the two motor terminals to power the motor in a reverse direction; and in the off position, electrically separates at least one of the two power terminals from the two motor terminals.

117. The instrument according to claim 115, wherein:
the motor has a permanent magnetic field; and at least one of the motor, the drive train, and the actuation assembly has an inertia-induced over-stroke characteristic after powered operation.

118. The instrument according to claim 117, wherein the inertia-induced over-stroke of at least one of the motor, the drive train, and the actuation assembly is counteracted with the short-circuit.

119. The instrument according to claim 117, wherein the short-circuit slows the still-spinning motor at a rate that substantially eliminates the inertia-induced over-stroke of at least one of the motor, the drive train, and the actuation assembly.

120. A surgical instrument, comprising:
a surgical end effector having at least one actuation assembly to effect a surgical procedure when actuated;
a handle mechanically coupled with the end effector and having a shell;
an electric motor disposed within the shell and having:

a rotational inertia when spinning;
a permanent magnetic field;
motor terminals; and a drive train operatively coupled to the at least one actuation assembly to actuate the at least one actuation assembly when the motor is supplied with power, the drive train having a rotational inertia when operating;
a power supply having power terminals; and a post-termination braking circuit:
having a selective switching connection disposed within the shell and having a break-before-make switch with three positions including a forward position, a reverse position, and an off position, the selective switching connection:
in the forward position, electrically connecting the power terminals to the motor terminals to power the motor in a forward direction;
in the reverse position, electrically connecting the power terminals to the motor terminals to power the motor in a reverse direction; and in the off position, electrically separating at least one of the power terminals from the motor terminals;
electrically short-circuiting the motor terminals with the off position of the switch; and being operable to create an electrically-generated magnetic field in opposition to the permanent magnetic field with the rotational inertia of at least one of the drive train and the motor when short-circuiting the motor terminals with the off position of the switch.

121. The instrument according to claim 120, wherein:
the power supply is a removable battery pack and has two power terminals; and the switch of the selective switching connection is a double-pole/double-throw, break-before-make switch with three positions including the forward position, the reverse position, and the off position, and:
in the forward position, electrically connects the two power terminals to the two motor terminals to power the motor in a forward direction;
in the reverse position, electrically connects the two power terminals to the two motor terminals to power the motor in a reverse direction; and in the off position, electrically separates at least one of the two power terminals from the two motor terminals.

122. A surgical instrument, comprising:
a surgical end effector;
at least one actuator mechanically coupled to the end effector for actuating the end effector;
a handle:
mechanically coupled to the end effector; and having an electric motor disposed therein and operable to actuate the at least one actuator when the motor is supplied with power;
a post-termination braking circuit including a power supply switch at the handle, the power supply switch having:
a break-before-make switch configuration;
a power-supplying state in which power is supplied to the motor; and a power-removed state in which power is not supplied to the motor, the post-termination braking circuit operable to short-circuit the power supplied to the motor when the power supply switch is in the power-removed state.

123. The surgical instrument according to claim 122, wherein the electric motor includes:
pow er terminals at which the motor is supplied with power; and a drive train operatively coupled to the at least one actuator to actuate the at least one actuator when the motor is supplied with power, wherein the post-termination braking circuit is operable to short-circuit the power terminals of the motor when the power supply switch is in the power-removed state.

124. The surgical instrument according to claim 122, wherein the handle further includes a power supply disposed therein and electrically connected to the motor through the post-termination braking circuit.

125. The surgical instrument according to claim 124, wherein the power supply is a removable battery pack.

126. The surgical instrument according to claim 122, wherein the power supply switch is a three-position switch including:
a forward position in which the three-position switch is in the power-supplying state and is configured to cause the motor to rotate in a forward direction;
a reverse position in which the three-position switch is in the power-supplying state and is configured to cause the motor to rotate in a reverse direction; and an off position in which the three-position switch is in the power-removed state and the motor is caused to prevent rotation at the motor.

127. The surgical instrument according to claim 123, wherein the drive train has a rotational inertia when operating;
the motor has:
a rotational inertia when spinning; and a permanent magnetic field; and the post-termination braking circuit is operable to create an electrically-generated magnetic field in opposition to the permanent magnetic field with the rotational inertia of at least one of the drive train and the motor when short-circuiting the power terminals.

128. The surgical instrument according to claim 122, wherein the power supply switch is a double-pole, double throw switch.

129. The surgical instrument according to claim 122, wherein the end effector, the handle, the motor, the power supply switch, and the post-termination braking circuit are all operable with only a single hand.

130. A method for post-termination braking of an electrical motor in an electrically powered surgical instrument, which comprises:
coupling a surgical end effector to a handle, the end effector having at least one actuator to effect a surgical procedure, and the handle having an electric motor disposed therein;
mechanically coupling the motor to the at least one actuator;
actuating the at least one actuator by selectively supplying the motor with power with a break-before-make power supply switch of a post-termination braking circuit, the power supply switch having an off state that ceases supply of power to the motor;
and upon ceasing supply of power to the motor, short-circuiting power terminals of the still-spinning motor with the off state of the power supply switch.

131. The method according to claim 130, wherein:
the step of mechanically coupling the motor to the at least one actuator is carried out by mechanically coupling a drive train of the motor to the at least one actuator;
the motor has a permanent magnetic field;
at least one of the motor, the drive train, and the at least one actuator has an inertia-induced over-stroke characteristic after powered operation; and the step of short-circuiting the power terminals of the motor creates an electrically generated magnetic field in opposition to the permanent magnetic field.

132. The method according to claim 131, further comprising counteracting the inertia-induced over-stroke of at least one of the motor, the drive train, and the at least one actuator with the short-circuit.

133. The method according to claim 131, further comprising carrying- out the short-circuiting step to slow the still-spinning motor at a rate that substantially eliminates the inertia-induced over-stroke of at least one of the motor, the drive train, and the at least one actuator.

134. The method according to claim 131, further comprising providing a power supply within the handle and electrically connecting the power supply to the motor.

135. The method according to claim 134, wherein the power supply is a removable battery pack.

136. The method according to claim 134, further comprising carrying out the short-circuiting step without short-circuiting the power supply.

137. The method according to claim 131, further comprising:
providing a power supply within the handle and electrically connecting the power supply to the motor; and carrying out the short-circuiting step without short-circuiting the power supply.

138. The method according to claim 131, wherein the break-before-make power supply switch is a double-pole, double throw switch.

139. A surgical stapling instrument, comprising:

a handle having a stapler-closing device;
a surgical stapling end effector connected to the handle and having a pair of opposing stapling surfaces, at least one of the stapling surfaces operable to move with respect to the other of the stapling surfaces upon actuation of the stapler-closing device to apply a compressive force to tissue therebetween; and a mechanical force switch operable to receive the compressive force applied to the tissue and to exhibit at least one of mechanical and electrical change associated with the received compressive force, the at least one change influencing a surgical procedure on the compressed tissue.

140. The surgical stapling instrument according to claim 139, wherein the surgical stapling end effector further comprises a knife assembly disposed to cut the compressed tissue between the stapling surfaces.

141. The surgical stapling instrument according to claim 139, wherein the at least one mechanical and electrical change exhibited by the mechanical force switch is dependent upon the compressive force received being at least equal to a pre-determined compressive force.

142. The surgical stapling instrument according to claim 141, wherein the pre-determined compressive force is a biasing force that opposes the compressive force received.

143. The surgical stapling instrument according to claim 142, wherein the pre-determined compressive force is applied by a pre-loaded spring.

144. The surgical stapling instrument according to claim 141, wherein the pre-determined compressive force is dependent upon at least one of a kind and an amount of tissue to be compressed prior to stapling the compressed tissue.

145. The surgical stapling instrument according to claim 141, wherein the pre-determined compressive force is dependent upon an acceptable staple-forming range.

146. The surgical stapling instrument according to claim 141, wherein the pre-determined compressive force is adjustable to accommodate differences in tissue thicknesses.

147. The surgical stapling instrument according to claim 139, wherein:
the handle has a longitudinal axis; and the mechanical force switch is disposed along the longitudinal axis.

148. The surgical stapling instrument according to claim 147, wherein the mechanical force switch is operable to switch from a first switching state to a second switching state.

149. The surgical stapling instrument according to claim 148, wherein the surgical stapling end effector carries out the surgical procedure on the compressed tissue only after the compressive force received by the mechanical force switch is sufficient to change the mechanical force switch from the first switching state to the second switching state.

150. The surgical stapling instrument according to claim 139, wherein the surgical stapling end effector comprises one of a circular surgical staple head and a linear surgical staple head.

151. The surgical stapling instrument according to claim 139, further comprising an electric indication circuit electrically connected to the mechanical force switch and operable to produce a signal indicating occurrence of the at least one mechanical and electrical change.

152. The surgical stapling instrument according to claim 139, further comprising an electric indication circuit electrically connected to the mechanical force switch and operable to produce a signal indicating an amount of compressive force applied to the tissue.

153. A surgical stapling instrument, comprising:
a handle having a stapler-closing device;
a surgical stapling end effector connected to the handle and having a pair of opposing stapling surfaces, at least one of the stapling surfaces operable to move with respect to the other of the stapling surfaces upon actuation of the stapler-closing device to apply a compressive force to tissue therebetween;
a mechanical force switch operable to receive the compressive force applied to the tissue and to switch from a the first electrical switching state to a second electrical switching state, the first and second electrical switching states being initiated and changed solely by mechanical movements associated with the received compressive force, the change in electrical switching states influencing a surgical procedure on the compressed tissue; and the change in electrical switching states being dependent upon the received compressive force being at least equal to a pre-determined compressive force, wherein the pre-determined compressive force is a biasing force that retains the mechanical force switch in the first electrical switching state until the opposing the compressive force received upon the mechanical force switch overcomes the biasing force to change the mechanical force switch to the second electrical switching state.

154. A surgical stapling instrument, comprising:
a handle having a stapler-closing device and a longitudinal axis;

a surgical stapling end effector connected to the handle and having a pair of opposing stapling surfaces, at least one of the stapling surfaces operable to move with respect to the other of the stapling surfaces upon actuation of the stapler-closing device to apply a compressive force to tissue therebetween;
a mechanical force switch disposed along the longitudinal axis of the handle, the mechanical force switch being operable to receive the compressive force applied to the tissue and to exhibit at least one of mechanical and electrical change associated with the received compressive force, the at least one change influencing a surgical procedure on the compressed tissue; and an electric indication circuit electrically connected to the mechanical force switch and operable to produce a signal indicating occurrence of the at least one of mechanical and electrical change.

155. The surgical stapling instrument according to claim 154, wherein the mechanical force switch is operable to switch from a first electrical switching state to a second electrical switching state, the first and second electrical switching states being initiated and changed solely by mechanical movements associated with the received compressive force.

156. The surgical stapling instrument according to claim 155, wherein the surgical stapling end effector carries out the surgical procedure on the compressed tissue only after the compressive force received by the mechanical force switch is sufficient to change the mechanical force switch from the first electrical switching state to the second electrical switching state.

157. The surgical stapling instrument according to claim 155, wherein the change in electrical switching states of the mechanical force switch is dependent upon the compressive force received being at least equal to a pre-determined compressive force, wherein the pre-determined compressive force is a biasing force that opposes the compressive force received.

158. The surgical stapling instrument according to claim 153, further comprising an electric indication circuit electrically connected to the mechanical force switch and operable to produce a signal indicating at least one of:
occurrence of the change in electrical switching states; and an amount of compressive force applied to the tissue.

159. An electrically operated surgical instrument, comprising:
a handle having:
a power supply;
a drive assembly having:
an electrically powered motor;
a controller electrically connected to the power supply and to the motor and selectively operating the motor; and a drive part selectively moved by the motor between a fully extended position and a fully retracted position upon actuation of the motor; and a control assembly operably connected to the motor to control a direction of rotation of the motor and operably connected to the controller to control power supplied to the motor;
a surgical end effector connected to the handle and having:

a pair of opposing compression surfaces, at least one of the pair of opposing compression surfaces being operable to move with respect to the other of the pair of opposing compression surfaces to apply a compressive force to tissue therebetween; and a tissue-cutting assembly comprising:
a blade moving with the drive part to pass between the opposing compression surfaces over the course of a blade stroke and thereby cut tissue compressed between the pair of compression surfaces, the blade stroke including a retracted position of the blade; and the control assembly being operable to selectively cause the motor to automatically retreat the drive part to place the blade in the retracted position of the blade.

160. The instrument according to claim 159, wherein the control assembly is operable to selectively cause the motor to automatically retreat the drive part to the fully retracted position and stop at the fully retracted position.

161. The instrument according to claim 159, wherein the blade stroke is comprised of the drive part advancing the blade distally towards the tissue to an extended position of the blade and retreating the blade proximally to a retracted position of the blade.

162. The instrument according to claim 159, wherein the power supply is a removable battery pack containing at least one battery.

163. The instrument according to claim 159, wherein:
the first of the pair of opposing compression surfaces is an anvil having a staple-forming surface; and the second of the pair of opposing compression surfaces is a surgical staple cartridge assembly operable to eject at least one surgical staple contained therein opposite the staple-forming surface of the anvil.

164. The instrument according to claim 159, wherein the control assembly is a switch assembly comprising:
a first switch operably disposed to switch when the drive part is at the fully retracted position; and a second switch operably disposed to switch when the drive part is at the fully extended position.

165. The instrument according to claim 164, wherein the second switch is operatively connected to the control assembly and, when switched due to advancement of the drive part to the fully extended position, causes the motor to automatically retract the drive part backwards from the fully extended position.

166. The instrument according to claim 165, wherein:
the second switch is operatively connected to the control assembly and, when switched due to advancement of the drive part to the fully extended position, causes the motor to automatically retract the drive part backwards to the fully retracted position; and the first switch is operatively connected to the control assembly and, when switched due to retraction of the drive part to the fully retracted position after having reached the fully extended position, causes the control assembly to remove power from the motor and stop any further movement of the drive part towards the fully extended position.

167. The instrument according to claim 216, wherein:

the tissue-cutting assembly is a staple-firing and tissue-cutting assembly comprising a surgical staple cartridge containing surgical staples operatively connected to at least one of the blade and the drive part; and activation of the second switch by the drive part at the fully extended position operates to stop further staple firing by the staple-firing and tissue-cutting assembly.

168. The instrument according to claim 163, wherein:
the surgical staple cartridge assembly has a staple-ejecting surface;
a distance between the staple-forming surface of the anvil and the staple-ejecting surface of the surgical staple cartridge assembly defines an anvil-cartridge gap; and the handle further comprises an anvil control assembly having:
a second electrically powered motor electrically connected to the controller and selectively operated by the controller;
a drive rod selectively moved by the second motor to advance the anvil distally towards the surgical staple cartridge assembly and to retract the anvil proximally away from the surgical staple cartridge assembly between a proximal-most position and a distal-most position when driven by the second motor;
a first anvil switch operably disposed to switch when the drive rod is at the proximal-most position;
a second anvil switch operably disposed to switch when the drive rod is at the distal-most position;

a third anvil switch operably disposed to switch when the drive rod is at an intermediate position between the proximal-most and distal-most positions of the drive rod; and a fourth anvil switch operably disposed to switch then the drive rod is at a staple-fire ready position between the intermediate position and the distal-most position of the drive rod.

169. The instrument according to claim 168, wherein the intermediate position of the drive rod corresponds to placement of the anvil with respect to the surgical staple cartridge assembly for which the anvil-cartridge gap is within a safe staple firing range.

170. The instrument according to claim 169, wherein the safe staple firing range of the anvil-cartridge gap is approximately 1 centimeter.

171. The instrument according to claim 168, wherein advancement of the drive rod distally to:
the intermediate position activates the third anvil switch, at which point the anvil-cartridge gap is within a safe staple firing range;
the staple-fire ready position activates the fourth anvil switch, at which point at least one staple of the surgical staple cartridge assembly is permitted to be tired by the surgical staple cartridge assembly; and the distal-most position activates the second anvil switch, at which point the anvil-cartridge gap is no longer within a safe staple tiring range and power is removed from the motor to prevent any further staple firing by the staple-firing and tissue-cutting assembly.

172. The instrument according to claim 168, wherein retraction of the drive rod proximally to the proximal-most position activates the first anvil switch to remove power from the motor and to stop any further proximal movement of the drive rod.

173. The instrument according to claim 168, wherein the controller selectively operates at least one of the motor and second motor using pulse modulation.

174. An electrically operated surgical instrument, comprising:
a handle having:
a power supply;
a drive assembly having:
an electrically powered motor;
a controller electrically connected to the power supply and to the motor and selectively operating the motor; and a drive part selectively moved by the motor between a fully extended position and a fully retracted position upon actuation of the motor; and a control assembly operably connected to the motor to control a direction of rotation of the motor and operably connected to the controller to control power supplied to the motor;
a surgical end effector connected to the handle and having:
a pair of opposing compression surfaces, at least one of the pair of opposing compression surfaces being operable to move with respect to the other of the pair of opposing compression surfaces to apply a compressive force to tissue therebetween; and a tissue-cutting assembly comprising:
a blade connected to the drive part to pass between the opposing compression surfaces over the course of a blade stroke and thereby cut tissue compressed between the pair of compression surfaces, the blade stroke being comprised of the drive part advancing the blade distally towards the tissue to an extended position of the blade and retreating proximally to a retracted position of the blade; and the control assembly being operable to selectively cause the motor to automatically retreat the drive part to place the blade in the retracted position of the blade.

175. A hand-held, electrically powered and controlled surgical device, comprising:
a handle shaped to be held within one hand of a user, the handle having:
a self-contained electric power source;
at least part of an end effector control assembly electrically connected to the power source;
a switch electrically connected to the power source and operable to selectively power the end effector control assembly with the power source; and an articulation control device, wherein the switch and the articulation control device are configured to permit operation of both with the one hand of the user that is holding the handle;

an articulating connection operable to articulate upon operation of the articulation control device; and a surgical end effector:
connected to the handle by the articulating connection such that articulation of the surgical end effector is controlled by operation of the articulation control device; and operatively connected to the end effector control assembly such that, upon operation of the end effector control assembly, the surgical end effector is operable to carry out at least one electrically powered surgical procedure.

176. The device according to claim 175, wherein the surgical end effector is operable to carry out the at least one surgical procedure w hen the switch is selected to power the end effector control assembly.

177. The device according to claim 175, wherein the power source is comprised of at least one battery cell.

178. The device according to claim 177, wherein the at least one battery cell is a lithium-based battery cell.

179. The device according to claim 175, wherein the surgical end effector is a stapling and cutting surgical end effector operable to staple and cut tissue disposed at the surgical end effector upon operation of the end effector control assembly.

180. The device according to claim 179, wherein the end effector control assembly is comprised of:
at least part of an anvil control assembly; and at least part of an electrically-powered stapler control assembly electrically connected to the power source.

181. A hand-held, electrically powered and controlled surgical device, comprising:
a handle shaped to be held within one hand of a user, the handle having:
a self-contained electric power source;
at least part of an end effector control assembly electrically connected to the power source, the end effector control assembly comprising:
at least part of an anvil control assembly; and at least part of an electrically-powered stapler control assembly electrically connected to the power source;
a switch electrically connected to the power source and operable to selectively power the end effector control assembly with the power source; and an articulation control device, wherein the switch and the articulation control device are configured to permit operation of both with the one hand of the user that is holding the handle;
an articulating connection operable to articulate upon operation of the articulation control device; and a surgical end effector:
connected to the handle by the articulating connection such that articulation of the surgical end effector is controlled by operation of the articulation control device; and operatively connected to the end effector control assembly such that, upon operation of the end effector control assembly, the surgical end effector is operable to staple tissue disposed at the surgical end effector.

182. The device according to claim 181, wherein the surgical end effector is operable to carry out a staple procedure when the switch is selected to power the end effector control assembly.

183. The device according to claim 181, wherein the surgical end effector comprises:
an anvil operatively connected to the at least part of the anvil control assembly; and a stapler operatively connected to the at least part of the stapler control assembly, the stapler positioned opposite the anvil such that, together, the stapler and the anvil are operable to staple tissue disposed therebetween.

184. The device according to claim 183, wherein:
the anvil control assembly is operable to selectively close the anvil and compress the tissue disposed between the stapler and the anvil; and the switch is operable to selectively power the at least part of the stapler control assembly such that the stapler carries out a staple procedure upon the compressed tissue when the switch is selected to power the stapler control assembly.

185. The device according to claim 181, wherein the power source is comprised of at least one battery cell.

186. The device according to claim 185, wherein the at least one battery cell is a lithium-based battery cell.

187. A hand-held, electrically powered and controlled surgical device, comprising:
a handle shaped to be held within one hand of a user, the handle having:
a self-contained electric power source;
at least part of an end effector control assembly electrically connected to the power source, the end effector control assembly comprising:
at least part of an anvil control assembly; and at least part of an electrically-powered stapler control assembly electrically connected to the power source;
a switch electrically connected to the power source and operable to selectively power the end effector control assembly with the power source; and an articulation control device, wherein the switch and the articulation control device are configured to permit operation of both with the one hand of the user that is holding the handle;
an articulating connection operable to articulate upon operation of the articulation control device; and a surgical end effector:
connected to the handle by the articulating connection such that articulation of the surgical end effector is controlled by operation of the articulation control device; and comprising:
an anvil operatively connected to the at least part of the anvil control assembly; and a stapler operatively connected to the at least part of the stapler control assembly, the stapler positioned opposite the anvil such that, together, the stapler and the anvil are operable to staple tissue disposed therebetween upon operation of the end effector control assembly.

188. The device according to claim 187, wherein the surgical end effector is operable to carry out a staple procedure when the switch is selected to power the end effector control assembly.

189. The device according to claim 187, wherein:
the anvil control assembly is operable to selectively close the anvil and compress the tissue disposed between the stapler and the anvil; and the switch is operable to selectively pow er the at least part of the stapler control assembly such that the stapler carries out a staple procedure upon the compressed tissue when the switch is selected to power the stapler control assembly.

190. The device according to claim 187, wherein the power source is comprised of at least one battery cell.

191. The device according to claim 190, wherein the at least one battery cell is a lithium-based battery cell.