WO2011097672A1 - Suture anchor - Google Patents
Suture anchor Download PDFInfo
- Publication number
- WO2011097672A1 WO2011097672A1 PCT/AU2011/000131 AU2011000131W WO2011097672A1 WO 2011097672 A1 WO2011097672 A1 WO 2011097672A1 AU 2011000131 W AU2011000131 W AU 2011000131W WO 2011097672 A1 WO2011097672 A1 WO 2011097672A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- holding element
- suture
- hollow body
- bone
- hollow
- Prior art date
Links
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
- A61B17/04—Surgical instruments, devices or methods, e.g. tourniquets for suturing wounds; Holders or packages for needles or suture materials
- A61B17/0401—Suture anchors, buttons or pledgets, i.e. means for attaching sutures to bone, cartilage or soft tissue; Instruments for applying or removing suture anchors
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
- A61B17/04—Surgical instruments, devices or methods, e.g. tourniquets for suturing wounds; Holders or packages for needles or suture materials
- A61B17/0482—Needle or suture guides
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
- A61B17/16—Bone cutting, breaking or removal means other than saws, e.g. Osteoclasts; Drills or chisels for bones; Trepans
- A61B17/17—Guides or aligning means for drills, mills, pins or wires
- A61B17/1739—Guides or aligning means for drills, mills, pins or wires specially adapted for particular parts of the body
- A61B17/1778—Guides or aligning means for drills, mills, pins or wires specially adapted for particular parts of the body for the shoulder
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
- A61B17/16—Bone cutting, breaking or removal means other than saws, e.g. Osteoclasts; Drills or chisels for bones; Trepans
- A61B17/17—Guides or aligning means for drills, mills, pins or wires
- A61B17/1796—Guides or aligning means for drills, mills, pins or wires for holes for sutures or flexible wires
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
- A61B17/16—Bone cutting, breaking or removal means other than saws, e.g. Osteoclasts; Drills or chisels for bones; Trepans
- A61B17/17—Guides or aligning means for drills, mills, pins or wires
- A61B17/1714—Guides or aligning means for drills, mills, pins or wires for applying tendons or ligaments
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
- A61B17/04—Surgical instruments, devices or methods, e.g. tourniquets for suturing wounds; Holders or packages for needles or suture materials
- A61B17/0401—Suture anchors, buttons or pledgets, i.e. means for attaching sutures to bone, cartilage or soft tissue; Instruments for applying or removing suture anchors
- A61B2017/0409—Instruments for applying suture anchors
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
- A61B17/04—Surgical instruments, devices or methods, e.g. tourniquets for suturing wounds; Holders or packages for needles or suture materials
- A61B17/0401—Suture anchors, buttons or pledgets, i.e. means for attaching sutures to bone, cartilage or soft tissue; Instruments for applying or removing suture anchors
- A61B2017/0446—Means for attaching and blocking the suture in the suture anchor
- A61B2017/0448—Additional elements on or within the anchor
- A61B2017/045—Additional elements on or within the anchor snug fit within the anchor
Definitions
- This invention relates generally to an apparatus used in the securement of the position of a suture.
- Arthroscopic surgical techniques are at this time increasingly preferred for multiple reasons, such as increased access and potential ease of use of surgical elements during surgery, less disturbance of the patient's body organs and tissues, and typically reduced recovery periods (of particular importance to sports persons) during which there is less discomfort for the patient.
- a wide range of anchors are used for glenohumeral instability, superior labrum
- Anchors including a screw portion are known for providing a mechanical bond to bone.
- this type of anchor can typically only be inserted in one action and does not provide for adjustability of depth or angle.
- Another approach to bone anchor design uses a split hollow shaft inserted into a hole created in the cortical bone.
- the anchor carries a tapered plug extending through the full length of the hollow shaft of the anchor with the broadest end of the inner end (with respect to the bone) of the shaft located such that when the plug is pulled towards the outer end of the shaft the tapered portion of the plug causes the hollow shaft body to flare radially outward effectively locking the device into the cortical bone structure.
- This type of anchor also needs to be inserted in one action and does not provide for adjustability of depth or angle.
- Anchors of the type described in the previous paragraph can be used in suitable bones, and if used in conjunction with sutures, will fixedly incorporate typically two or more lengths of suture material which are then available for attachment to the relevant tissue and securely knotted as required.
- An alternative is to provide an eyelet on the outer end of the anchor through which suture material can be threaded and/or tied to.
- a problem with such anchor types is that the eyelet can break or unduly abrade the suture material in addition to the time and skill involved in placing the suture material into the soft tissue, looping through the anchor eyelet, and tying knots wherein all these procedures are done during arthroscopic surgery.
- This type of anchor also is preferably inserted in one action and does not provide for adjustability of depth or angle.
- an arthroscopic transosseous knotless suture anchoring arrangement for holding a suture with respect to a cortical portion of a bone, includes, a hollow body for at least partial insertion into a cortical portion of a bone; and a holding element having an elongate body sized for fitment with and within the hollow of the body for holding a portion of a suture located in the hollow body with respect to the cortical portion of the bone.
- a device for capturing and holding a suture under tension with respect to a cortical bone portion includes, a hollow elongate body having an inner surface forming the hollow, at least a portion of the body for placement in a cavity located in the cortical bone portion, the hollow body having a rim radially extending from one end of the body, the rim adapted to receive a force that forces at least a portion of the rim to abut the cortical bone adjacent to the cavity in the cortical bone; and a holding element sized for fitment with and within the hollow of the body; wherein a portion of the suture is located within the hollow body and while, the free end of the suture is under tension caused by a force on the suture applied in a direction away from the outer surface of the cortical bone, and another force in substantially the opposite direction is applied to the rim of the body, the holding element is interference fitted into the hollow body so as to capture a portion of the suture under tension which is located within the hollow body while
- Figure 1 depicts a breakaway anterior view of a muscular-skeletal view of a rotator cuff of a human
- Figure 2 depicts a breakaway view of a torn rotator cuff
- Figure 3 depicts a suture attachment to the rotator cuff through a lateral skin aperture
- Figure 4 depicts inspection and possible preparation of the top of the humerous through the lateral skin aperture including the making of a hole or trench in a humerus bone;
- Figure 5 depicts a suture transfer guide instrument being inserted through one of the arthroscopic skin apertures and into a hole in the upper humerus, and being positioned in preparation for creating the lateral humeral hole;
- Figure 6 depicts the trochar and suture retrieval sleeve being positioned and about to be inserted into the guiding sleeve on the outer arm of the suture transfer guide;
- Figure 7 depicts the trochar inserted into the suture retrieval sleeve and about to be inserted into the guiding sleeve on the outer arm of the suture transfer guide;
- Figure 8 depicts the suture retrieval sleeve with its trochar being advanced though the lower skin aperture, through a hole in the lateral aspect of the humerus and into the humeral bone medulla to a point adjacent to the intra-osseous portion of the suture transfer guide;
- Figure 9 depicts the withdrawal of the trochar, leaving the suture retrieval sleeve in place
- Figure 10 depicts the suture transfer guide in place with the suture retrieval sleeve in place adjacent to the foramen at the distal portion of the intra-osseous portion of the guide;
- Figure 11 depicts the threading of a guide thread through the central hole in the intra-osseous portion of the suture transfer guide and then out through the suture retrieval sleeve so it passes through both holes in the humerus;
- Figure 12 depicts the withdrawal of the suture retrieval sleeve, but leaving the guide thread in place
- Figure 13 depicts the removal of the intra-osseous arm of the guide suture transfer from the humerus, taking care that the guide thread remains in place;
- Figure 1 depicts the disengagement of the suture transfer guide from the guide thread
- Figure 15 depicts both the suture attached to the rotator cuff and the guide thread threaded through the bone;
- Figure 16 depicts the suture after being pulled through the hole in the bone still attached to the rotator cuff
- Figure 17 depicts the rotator cuff being pulled by the suture through one of the holes in the bone
- Figure 18 depicts the threading of a hollow body over the suture
- Figure 19 depicts the embedding of the hollow body into the bone
- Figure 20 depicts the placement of a holding element through one of the two lateral skin openings towards the hollow body;
- Figure 21 depicts the placement of the holding element into the hollow body;
- Figure 22 depicts fitment of the holding element and the repair suture/s within the hollow body, and with the sutures divided at the outer surface of the holding body;
- Figure 23 depicts a guide to assist the feeding of the holding element into the hollow body using a plug and the guide also impacting the hollow body into the bone.
- Figure 24 depicts pictorial representations of a holding element and a hollow body
- Figure 25 depicts a pictorial representation of the positioning of the holding element while two sutures are threaded through the hollow body
- Figure 26 depicts a pictorial representation of the insertion of the holding element into the hollow body capturing the sutures
- Figure 27 depicts a pictorial representation of the fitted position of the holding element within the hollow body, and capturing the repair sutures.
- the devices described herein are useable to secure sutures in bone. There are many applications for the devices disclosed which are within the skill of a surgeon to determine. However, there is only one example of the use of the devices disclosed herein, which relates to the repair and remediation of damage to the rotator cuff using arthroscopic surgical procedures.
- the rotator cuff comprises muscles and their tendons including the subscapularis, supraspinatus, infraspinatus and teres minor, which surround the shoulder and connect between the humerus and the scapula. They will attach along the head of the humerus and their primary role is to help stabilise the shoulder during active movement, which is generally under the action of the deltoid muscle.
- All the muscles must work together, contracting and relaxing in synchronisation in order to provide a stable and mobile shoulder through the required range of motion.
- the stated procedures used by way of example herein include tensioning and positioning of the pathologically detached rotator cuff back on to prepared bone.
- Figure 1 depicts a breakaway anterior view of a muscular-skeletal view of a rotator cuff of a human.
- the rotator cuff group of muscles is depicted at 10 with the subscapularis 12 and supraspinatus 14 as shown in Figure 1.
- Figure 2 depicts a breakaway view of a torn rotator cuff wherein the supraspinatus 14 is shown partially separated from the humerus 16.
- arthroscopic surgery is to be used and in preparation for the surgery, openings in the skin of the patient are made through which the various procedures are conducted.
- a pictorial representation of the aperture is shown as 18.
- Both an high skin aperture 18 ( Figures 3 and 4) and lower on the upper arm skin an aperture 29 is shown in Figure S and these apertures remain the only access to the deeper tissues and humerus during the procedure.
- Figure 3 depicts a suture attachment to the torn tendon of the infraspinatus muscle of the rotator cuff muscles showing in particular the suture 19 drawn to the exterior of the patient through the aperture 18 to be external to the patient's body. Later in the procedure a suture or guide thread 28 will also be drawn out through the high skin aperture 18, which will allow the guide thread to be attached to the repair suture 19 as detailed below.
- Figure 4 depicts inspection and possible preparation of the top of the humerous through the lateral skin aperture 18 and includes the making preparations for the making of a hole or trench in the humerus bone 16.
- Figure 5 depicts the preliminary step of making a hole or trench 20 in the upper region of the humerus, suitable to receive the suture transfer guide post 23.
- the hole 20 to be made is the first of two holes to be made in the humerus bone and the second hole needs to be made so as to meet up with the first hole inside the bone and thus to provide a passage through the bone.
- Figure 5 also pictorially illustrates how it is determined where both the first and second holes in the humerus bone should be made using a suture transfer guide instrument.
- the suture transfer guide instrument has a guide post 23 inserted through aperture 18 in the skin of the patient and then under arthroscopic visual control, inserted into the trench / first hole 20.
- the suture transfer guide instrument has an second guide arm 24 which is located parallel to the guide post 23 by the first guide arm 22, at a sufficient distance between the guide post 23 and the second guide arm 24 to allow for the thickness of soft tissue, including the deltoid muscle, subcutaneous fat and skin over the bone.
- a hollow cylindrical shaped attachment 25 At the bottom of the second guide arm 24 is a hollow cylindrical shaped attachment 25 at a right angle to the second guide arm 24 and of sufficient bore size and shape to allow passage of the longitudinal trochar 26 and suture retrieval sleeve 27a yet to be described.
- the guide post 23 has a bore its full length that is of sufficient size to allow easy passage of a guide thread 28 or suture that has stiffness sufficient to allow it to feed without coiling or kinking (by way of example, stiff plastic coated braided wire or thread).
- the hole at the bottom of the guide post 23 is at a right angle to the long axis of the guide post 23 and ' directed laterally towards the second guide arm 24 and specifically in line with the centre of the guiding sleeve 25.
- Placement of the guide post 23 within the intended hole 20 and positioning of the second guide arm 24 at or near the top of the humerus bone near where the second hole 27 ( Figure 8) in the humerus is to be created are a judgment call by the surgeon.
- the process of making the second hole 27 is achieved by placing a trochar 26 and suture retrieval sleeve 27a and guiding sleeve 25 and making the hole 27 in the numerous through the cortical bone as pictorially depicted in Figure 8.
- the trochar 26 and suture retrieval sleeve 27a is advanced within the humerus until in contact with the first post 23.
- the trochar 26 is then removed as is depicted in Figure 9 and the suture retrieval sleeve 27a left in place (Figure 10).
- stiff suture or fine guide thread 28 is inserted into the upper externally exposed hole of the guide post 23 and advanced into the bore.
- the suture or guide thread 28 advances through the suture retrieval sleeve 27a to exit at its lateral end.
- the suture or guide thread 28 is then advanced a sufficient distance to ensure it can be secured at both ends external of the body.
- the suture retrieval sleeve 27a is then withdrawn laterally until it clears the guiding sleeve 25 and is slid off the suture or guide thread 28, ensuring the suture or guide thread 28 remains present at both the upper 18 and lower 29 skin apertures (not shown).
- Figure 1 depicts a suture or guide thread 28 passing through the passage created by two holes in the humerous via the higher skin aperture 18 and lower skin aperture 29.
- the suture 19 which is attached to a tendon of the rotator cuff muscle group is then attached to the suture or guide thread 28 at its upper end, by either an in-line knot, or by passing the suture 19 through a braided snare section in the suture or guide wire 28 (Figure 15).
- the suture or guide wire 28 is drawn in a distal direction by pulling on the suture or guide wire 28 from externally of the lower skin aperture 29.
- the suture 19 is attached at the other end of the suture to a tendon of the rotator cuff muscle group.
- the suture and attached tendon is thus drawn back through to the first skin aperture 18 and further through the created bone tunnel beginning at 20.
- the sutures path then follows the tunnel and exits the body via the lower skin aperture 29 and external to the patient as illustrated in Figure 16 (which does not show the tendon attached to the other end of the suture.
- Figures 18 and 20 depict an arthroscopic transosseous knotless suture anchoring arrangement, including a hollow body and a suture holding element.
- the hollow body may also be referred to in this specification as an anchor.
- the hollow body 30 has an outer surface 31 which abuts the inside of the aperture 27 located in the cortical bone of the humerus 16 and thus is at least partially inserted into the cortical bone.
- one end of the hollow body 30 there is a rim 33 which radially extends from the hollow body.
- the rim 33 is adapted to receive a force on an outer (with respect to the bone and patient) by the provision in one embodiment of a force application surface 32 and thus the inner facing portion of the rim 33 (underside of the rim) to abut the outer surface of the humerus bone 16 adjacent and surrounding the bony cavity of second hole 27.
- Figures 19 and 20 only pictorially illustrate the hollow body 30 located in the humerus bone 16 with the free end 19 of the suture leading out of the centrally located aperture 34 (figure 19) of the hollow body 30 and the suture still visible within the bone, which if drawn true to life would not be the case.
- Figure 20 depicts a holding element 35 which is shaped and sized for fitment with and within the hollow of the body 30 which when fitted therein holds a portion of a suture 19 located within the hollow body with respect to the cortical bone within which the hollow body is at least partial inserted into.
- the holding element 35 can also be shaped and sized for interference fitment with and within the hollow of the body 30 which may be achieved by slightly oversizing the holding element with respect to the interior shape of the hollow in the hollow body.
- the holding element 35 can also be shaped and sized for interference fitment with and within the hollow of the body 30 by having closely complementary shapes of the outside of the holding element and the inside of the hollow element still slightly oversizing the holding element with respect to the interior shape of the hollow in the hollow body but he surfaces are not planar and could include tangs and tabs with sufficient give to allow for one way fitment.
- the holding element 35 can also be shaped and sized for removeable fitment with and within the hollow of the body 30 which may be achieved using the oversizing arrangement described above or by allowing one way fitment and a reverse release arrangement, such as tangs and tabs which interact to provide such engagement and release into and out of the interior shape of the hollow in the hollow body.
- a shape provided in a preferred embodiment of the invention consists of the hollow in the body 30 in the form of a single wall of circular cross-section along the longitudinal axis of the body 30 having its largest internal diameter on the rim end of the body and its smallest internal diameter at the other end of the body.
- the holding element 35 preferably has a complementary shape, so as to provide an interference fitment of the holding element to the hollow body sufficient to retain the holding element within the hollow body and also accommodate and secure at least a portion of a suture material within the hollow body (that is passing through the hollow body) at the same time.
- the circular cross-section of the internal hollow of the body and the outer surface of the holding element varies in diameter so as to taper (that is the radius varies at a constant rate along the length so that the side walls of both the hollow and the outer surface of the holding element are straight in lateral cross-section as illustrated at least in respect to the hollow body shown in Figure 24. While the outer surface of the holding element 35 is shown with ridges 36 in that same figure, more detail of which will be provided later in the specification.
- the holding element 35 should be removable from the hollow body 30 if required.
- the holding element can be removed, one of which includes the provision of an engagement surface on the surface which remains exposed to the surgeon even once the holding element has been fitted to hollow body.
- other extraction techniques which may be not unlike the extraction of a cork from a bottle, or others techniques can be employed as seen fit by the surgeon.
- the holding element 35 depicted in Figure 24 is itself hollow and an appropriately shaped tool can be inserted into the hollow to assist removal of a hollow element from the hollow body.
- PictoriaJly illustrated in Figure 21 is the result of the following steps. While a portion of the suture 19 is located within the hollow body 30 and while, the free end 19a of the suture 19 is under tension caused by a force on the suture applied in a direction away from the outer surface of the cortical bone, that force being applied by the surgeon pulling on the free end of the suture 19 with a sufficient force to bring the tendon into adjacency with the prepared surface of the bone, another force in substantially the opposite direction is applied to the force receiving portion 32 of the rim 33 of the hollow body 30, the holding element 35 is interference fitted into the hollow body so as to capture a portion of the suture 1 under tension and while the inner facing portion of the rim 31 of the hollow body abuts the cortical bone portion.
- the captured portion of the suture is thus held in place with respect to the outer surface of the cortical bone, thus anchoring the sutured tendon to a stable portion of the body.
- the fixing of the hollow body to the cortical portion of the bone is also assisted by the tension between the captured suture and the rotor cuff tendency to retract towards the muscle.
- a holding element delivery device 200 includes an elongate body with an internal longitudinal aperture the length of the device having an internal diameter larger that the largest outer diameter of a holding element.
- a recessed shape 204 (one view of which is shown in Figure 23) at one end of the holding element delivery device to allow interference fit of that end and temporary attachment to the periphery of the rim 32 of the hollow body 30, although this feature is only preferable for both holding the hollow body as it is inserted into the body and into the aperture in the bone and also to stabilise the union of the holding element delivery device and the partially inserted hollow body during the holding element fitment process.
- the tool 200 is used to guide the hollow body 30 through the skin aperture 29 and then into the lateral surgical access aperture second hole 27 in the humerus bone 1 , until the hollow body 30 contacts the outer cortical surface of the humerus with the underside of the rim 32.
- the application of suitable pressure from external of the body to the tool 200 allows for the firm placement of the hollow body into the humerus bone 16 by the surgeon.
- tension is placed on the suture 19 to ensure adequate advancement of the tendon of the rotator cuff muscle group into the first humeral hole 20.
- the holding element 35 is inserted into the open end of the guide 200 and pushed along the length of the holding element delivery device 200 with a holding element placement device 202, while as mentioned previously maintaining appropriate tension on the free end of the suture 19.
- the holding element placement device 202 in one embodiment has a length, and an outer diameter less than the smallest internal diameter of the holding element delivery device 200.
- the holding element delivery device has an end shaped to conform to at least a portion of the shape of the end of the hollow body external of the cortical portion of a bone.
- the holding element placement device includes at least one longitudinal channel on its outer surface shaped and sized to at least accommodate a suture.
- the holding element placement device includes at least two longitudinal channels on its outer surface shaped and sized to at least accommodate a suture in each channel.
- a desirable position of the two strands of the suture 19 is on opposite sides of the holding element 35, and a feature of the holding element placement device 202 is a channel on either side (not shown) to ensure the suture 1 stands are correctly positioned.
- the holding element placement device is provided with a mark or indicia 202a which indicate the length of the shaft that needs to be inserted into the holding element delivery device 200 so as to ensure that the holding element 35 is located within the hollow body 30. The amount offeree applied will be a judgement call by the surgeon.
- Figure 24 provides cross-sectional views of the hollow body 30 located in a cortical portion of a bone 16 and a holding element 35.
- the relative dimensions of the body and element are merely illustrative and should not limit the scope of the invention.
- the materials of which the hollow body and holding element are made are preferably biocompatible and may not be of the same material, colour, density, or hardness.
- the shape of the outer surface as shown in cross-section of an embodiment of the holding element 35 indicates the use of a plurality of ridges 36 along the length of the holding element.
- the ridges are only shown in cross-section and may extend all or only part the way about the outer surface of the element. At least a portion of one or more of the ridges contribute to the interference fit forces which restrain the dislodgement of the holding element from the hollow body as well as apply a holding force to the captured portion of the suture 19.
- Use of ridges of the configuration described above, or the use of ridges at all, is not essential as long as both forms of holding force are provided.
- the outline cross- sectional shape of the holding element substantially conforms to the inside shape of the hollow body which contributes to the application of the forces mentioned above.
- the holding element 35 it is hollow but this also is not an essential feature.
- the fitment may be of any type including of the interference type, the engagement type, and one or other of the fitments may allow the holding element to be removeable from the hollow body.
- Figure 25 depicts the bone 16 and the suture 19 and it's free end of 19a with the holding element 35 external of the hollow body 30.
- Figure 26 is merely illustrative of the fitment of the holding element 35 into the hollow body 30.
- Figure 27 depicts a placement configuration of the holding element 35 and hollow body 30 showing the capture of the suture 19 therein and the removal of the free ends of the suture 19a.
- Such an arrangement provides a substantially flat surface on the outer surface of the bone which is an improvement if not an alternative for the prior termination techniques for sutures, which required the free ends of the sutures to be tied off and thereby secured with multiple knots, which are proud of any associated anchor.
- Figure 27 shows the surgical result of the use of a device for capturing and holding a suture under tension with respect to a cortical bone. Surgical recovery is prescribed for each surgical patient and generally includes some weeks of the arm being kept in a sling to immobilize the repaired region as much as possible.
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Abstract
Description
Claims
Priority Applications (6)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US13/578,798 US20130144335A1 (en) | 2010-02-09 | 2011-02-09 | Suture anchor |
CN201180008833.7A CN102821708B (en) | 2010-02-09 | 2011-02-09 | suture anchor |
BR112012019959A BR112012019959A8 (en) | 2010-02-09 | 2011-02-09 | SUTURE ANCHORAGE |
JP2012552210A JP2013518688A (en) | 2010-02-09 | 2011-02-09 | Suture anchor |
EP11741747.7A EP2533714A4 (en) | 2010-02-09 | 2011-02-09 | Suture anchor |
AU2011214892A AU2011214892B2 (en) | 2010-02-09 | 2011-02-09 | Suture anchor |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AU2010900513 | 2010-02-09 | ||
AU2010900513A AU2010900513A0 (en) | 2010-02-09 | Suture anchor |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2011097672A1 true WO2011097672A1 (en) | 2011-08-18 |
Family
ID=44367053
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/AU2011/000131 WO2011097672A1 (en) | 2010-02-09 | 2011-02-09 | Suture anchor |
Country Status (7)
Country | Link |
---|---|
US (1) | US20130144335A1 (en) |
EP (1) | EP2533714A4 (en) |
JP (1) | JP2013518688A (en) |
CN (1) | CN102821708B (en) |
AU (1) | AU2011214892B2 (en) |
BR (1) | BR112012019959A8 (en) |
WO (1) | WO2011097672A1 (en) |
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US11311284B2 (en) | 2019-03-06 | 2022-04-26 | Speed Clip Solutions, LLC | Suture tensioning and securement device, system, and methods |
WO2023118562A1 (en) * | 2021-12-23 | 2023-06-29 | Orthofix S.R.L. | Orthopedic cable bone transport device and bone transport system comprising said device |
WO2024133885A1 (en) * | 2022-12-23 | 2024-06-27 | Orthofix S.R.L. | Orthopedic cable bone transport device and bone transport system comprising said device |
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EP2995269B1 (en) | 2008-10-23 | 2017-07-26 | Spinewelding AG | Augmentation device for anchoring objects in hard tissue |
CA2811331C (en) | 2010-09-24 | 2020-04-21 | Sportwelding Gmbh | Suture anchor and method for fixating a suture relative to hard tissue |
RU2741462C2 (en) | 2010-09-24 | 2021-01-26 | СпортУэлдинг ГмбХ | Suture anchor, a method and a kit for securing the suture material with respect to the hard tissue |
US9386976B2 (en) | 2011-01-28 | 2016-07-12 | Sportwelding Gmbh | Method and device for fixating a suture anchor with a suture in hard tissue |
US9782165B2 (en) | 2011-11-11 | 2017-10-10 | VentureMD Innovations, LLC | Transosseous attachment |
US10548585B2 (en) | 2011-11-16 | 2020-02-04 | VentureMD Innovations, LLC | Soft tissue attachment |
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Also Published As
Publication number | Publication date |
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BR112012019959A2 (en) | 2016-04-26 |
CN102821708B (en) | 2016-11-09 |
AU2011214892B2 (en) | 2014-01-23 |
EP2533714A4 (en) | 2015-05-13 |
BR112012019959A8 (en) | 2017-12-05 |
JP2013518688A (en) | 2013-05-23 |
EP2533714A1 (en) | 2012-12-19 |
CN102821708A (en) | 2012-12-12 |
US20130144335A1 (en) | 2013-06-06 |
AU2011214892A1 (en) | 2012-08-30 |
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