A suspensory fixation device includes a standing block at one end thereof and a set of at least two adjustable loops at the second end thereof. The standing block includes a rigid fixation member having a plurality of apertures forming at least one sheave and a becket. A single reeved fall, rigid fixation member, adjustable loops, and sliding knot form a block and tackle system. A suspensory fixation button includes a rigid body having a top side and a bottom side, a plurality of lobes extending radially from the center of the body, and at least one aperture through the body near the root of a lobe. A method of coupling a suspensory fixation button to a set of adjustable flexible loops includes passing each adjustable loop over an edge of an extension of the button from the top side to the bottom side.

According to some embodiments, an implant for correcting a deformity in or near a joint of a subject includes an implant body having an internal lumen, a suture side hole or window extending through a wall of the implant body and providing access to the internal lumen through an exterior of the implant body, a tension assembly comprising a first bone anchor and a second bone anchor, wherein the first and second bone anchors are configured to be placed on opposite sides of the implant body, and an adjustable suture loop coupling the first bone anchor to the second bone anchor, wherein at least a portion of the at least one adjustable suture loop is positioned within the internal lumen of the implant body.

A suture anchor includes a material having thermoplastic properties and is fixated in a hard tissue opening by liquefying at least part of this material and letting it penetrate into walls of the hard tissue opening. During the named fixation and preferably towards the end of it, the suture being held in a distal suture conduit is locked relative to the hard tissue by being clamped between the suture anchor and the wall of the hard tissue opening or by being clamped or braked through collapse of the suture conduit.

An anchorage device includes a substrate extending along a longitudinal axis between a first end having a first bonding area and an opposite second end having a second bonding area. The substrate has a third bonding area between the first and second bonding areas. Kits, systems and methods are disclosed.

The technology includes an anchor assembly for tissue repair having an open helical coil sleeve and a tip structure. The tip structure includes an aperture for passing a suture and a suture capture member for capturing a suture. The technology also includes an anchor driver for installing an anchor into bone. The anchor driver includes an outer shaft and a sleeve advancement member for advancing the sleeve as well as an inner shaft and a suture capture advancement member for advancing the suture capture member. The technology also includes a system for tissue repair having an anchor assembly and an anchor driver for installing the anchor assembly into bone.

A tissue repair assembly for attachment of tissue to bone or tissue to tissue having a soft anchoring implant 100 with a length of suture 120 there through for tensioning the implant and facilitating attachment of other tissue. The implant 100 is a soft, flexible, three-dimensional structure that has a resident volume 200. An inserter tube 310 facilitates the placement of the implant 100 into bone or adjacent soft tissue where it may be deployed. Upon deployment, the soft anchoring implant 100 shortens axially and expands radially, achieving a larger diameter than the hole through which it was placed, thus resisting pull out.

A closure device for closing an opening in tissue that includes a needle actuation handle that cooperates with a housing. A hollow needle is selectively movable by the needle actuation handle, the needle including a slot extending proximally from a distal end of the needle. A suture anchor is positioned within and selectively releasable from the slot and coupled to a suture. A portion of the suture anchor extends proximally along an outer surface of the needle as the needle is advanced through tissue adjacent the opening.

A 3-D printed titanium porous screw adapted for placement within a bone tunnel, where the screw comprises a top section with a plurality of step-tapered edges, a middle section with porous inner lattice structure, and a lower section with tip portion for insertion into a bone tunnel. The plurality of step-tapered edges increases insertion torque and provides enhanced bone-to-implant contact and improved bone incorporation. The porous inner lattice structure allows the ingrowth of a patient's own bone quality to lessen the chance of rejection and loss of strength. Manufacturing of the 3-D printed lattice bone suture may be based on pre-operative MRI and CT scans that may be transferred to a software program to determine the integrity of the tendon as well as the evaluation of the bones involved. This allows the screw with suture anchor to be patient-specific in terms of the lattice formation and placement of the screw.

The present disclosure relates generally to the field of medical devices for delivering artificial chordae tendineae in a patient. A system for adjusting tension in an artificial chordae tendineae includes an artificial chordae tendineae coupleable between a clip and an anchor. The clip is engageable with a leaflet of a heart valve while the anchor is engageable with a papillary muscle or heart wall. The anchor includes a body portion, and a locking portion coupleable with the artificial chordae tendineae and configured to allow movement of the artificial chordae tendineae in a first direction while preventing movement of the artificial chordae tendineae in a second direction opposite the first direction. An actuator is coupled to the locking portion for selectively releasing the locking portion to enable selective movement of the artificial chordae tendineae in the second direction.

Methods and devices are provided for anchoring suture to bone. In one exemplary embodiment, a suture anchor is provided that includes a proximal component, a distal component, and an intermediate component positioned between the distal component and the proximal component. The proximal and distal components can each be configured to move independent of one another and to move relative to the intermediate component. In this way, the proximal, intermediate, and distal components of the suture anchor can be configured to cooperate with one another to prevent removal of the suture anchor from a bone hole in which the suture anchor is disposed and to lock a suture relative to the suture anchor and to the bone hole.