A helicoil interference fixation system comprising: a helicoil comprising a helical body comprising a plurality of turns separated by spaces therebetween, the helical body terminating in a proximal end and a distal end, and at least one internal strut extending between at least two turns of the helical body; and an inserter for turning the helicoil, the inserter comprising at least one groove for receiving the at least one strut; the helicoil being mounted on the inserter such that the at least one strut of the helicoil is mounted in the at least one groove of the inserter, such that rotation of the inserter causes rotation of the helicoil.

Provided is a surgical instrument including a first holding member, a sleeve member, a linkage member, a second holding member, a hook member and an opening/closing member. The second holding member is pivotally connected to the first holding member and when the second holding member moves relative to the first holding member, the linkage member is moved inside the sleeve member so as to drive the opening/closing member to move relative to the hook member. Through the movement of the opening/closing member of the surgical instrument, surrounding soft tissues, blood vessels or nerves that have strayed into the hook member can be pushed out so as not to be damaged by the hook member during surgery.

A system and method for loading a suture construct on a soft tissue graft with a graft assembly. The graft assembly includes a frame with an opening extending between a proximal end and a distal end. The frame has a wall with a first side extending to a first edge and a second side extending to a second edge. A lumen extends between the first side and the second side and a plurality of channels extend through the wall between the first edge and the second edge. The graft assembly also includes a transverse hole extending through the proximal end of the frame and a pin removably inserted into the transverse hole.

An anchor for anchoring tensile members to bone includes: a housing having a hollow interior; a collet in the interior of the housing, having a central bore for accepting tensile members therethrough and an exterior surface, wherein the collet is configured to be swaged around the tensile members; a sleeve having opposed interior and exterior surfaces, the sleeve disposed in the hollow interior of the housing and positioned adjacent to the collet, so as to be movable between first and second positions; wherein at least one of the exterior surface of the collet and the interior surface of the sleeve is tapered and the sleeve and the collet are arranged such that movement of the sleeve from the first position to the second position will cause the collet to swage radially inwards around the tensile members; and a flange element, wherein the housing is pivotally mounted to the flange element.

A surgical kit for repairing a ligament includes suture tape configured to be positioned across the ligament from a fixed end of the ligament to a free end of the ligament. At least one anchor is configured to position over the ligament. An instrument is configure to secure the anchor to the bone.

A graft compression system for compressing soft tissue grafts used in connection with reconstructive surgery. The graft compression system includes an upper press body and lower press body, pivotally couple to one another, each having inner sides having a plurality of parallel semi-circular shaped channels formed thereon. The plurality of parallel semi-circular shaped channels have sequentially decreasing channel widths. The upper press body and said lower press body of the graft compression system are configured to pivot about a pivot pin such that the inner sides abut one another, and such that the two sets of semi-circular shaped channels are substantially aligned with one another so as to receive a graft for compression. A screw press barrel is attached to the lower press body, on a side opposite the pivot pin, and is configured to compress the upper press body and lower press body.

Various bone anchor assemblies and methods are provided for anchoring tissue to bone. In one embodiment, an anchor assembly for anchoring a tendon to bone is provided and includes a substantially cylindrical sheath having bone-engaging surface features formed on an external surface thereof, and having an inner lumen formed therein and extending from an open proximal end to a substantially closed distal. The substantially closed distal end includes at least one tendon anchoring feature extending distally therefrom and configured to facilitate anchoring of a tendon to bone. The anchor assembly further includes an expander having a generally elongate cylindrical configuration and being sized and shaped to be received within the inner lumen of the sheath.

A medical holding system and method are disclosed herein. The medical holding system, in an embodiment, includes a retainer and a pivot device having a plurality of arms. Each of the arms is configured to be engaged with the retainer. The medical holding system also includes a grasper configured to be coupled to the pivot device. The grasper is configured to grasp a portion of an implantable element, and the pivot device is configured to be pivoted relative to the retainer.

A surgical device for performing a repair of lacerated or ruptured tendons is disclosed. The surgical device comprises a tip or first end, a base or second end opposite to the first end, and a length between the first and second end configured to pass at least in part through a tendon sheath. The surgical device increases in diameter from the first end to the second end over at least a portion of the length. The second end is shaped to accommodate retracted proximal end of the damaged tendons. The second end is inserted into a flexor fibro-osseous tunnel configured to distend and enlarge its pathway. The second end is sutured to the retracted proximal end and towed via the fibro-osseous tunnel, thereby providing a gentle, guided, and non-traumatic passage of the flexor tendon and retrieving the retracted proximal end of the damaged flexor tendon simultaneously to the repair zone.

An example medical device is disclosed. The medical device includes a delivery shaft and a frame. The frame is coupled to the distal portion of the delivery shaft, and the frame includes a body portion and at least first and second arms. Each arm has a first end attached to the body portion and a second, free end opposite the first end. The frame includes tabs on the arms and body portion configured to removably couple to an implant. The tabs on the arms and body portion may extend in different directions.