A graft suspension device for suspending a ligament in a bone hole having a first loop and a second loop suspending from an 8-hole anchor, and a cradle at the opposite end of the loops to the anchor. The loose ends of the suture are routed through holes in the anchor separate from the loops and are joined together to form a single tail. A finger loop allows a surgeon to adjust the distance of the cradle from the anchor with the cradle staying centered with respect to the anchor as the distance is adjusted.

An anatomy-specific implant for neuroplastic surgery. The implant includes a soft tissue implant component designed within and adapted to replace or restore missing soft tissue in a skull, joint or spine of the patient, wherein the soft tissue implant component is adapted to be coupled by an interdigitated connection to a rigid component. The rigid component can be a skull implant adapted to replace missing cranial or vertebral bone, or healthy cranial or vertebral bone, either of which can have downward extending catheters for medicinal brain or spinal cord infusion to help bypass the blood-brain barrier via multiphase flow. The soft tissue implant may include a functional component having neurotechnologies such as MRI-lucent pumps, Bluetooth connection systems, refillable diaphragms, remote imaging devices, wireless charging capabilities, and/or informative biosensors. The soft tissue implant component may be interchangeable with another soft tissue implant component in plug-and-play fashion.

The present disclosure relates to a fixation device. The fixation device includes a base portion having a first leg, a second leg, and a groove located between the first and second legs, and a top portion extending from the base portion. A method of tissue repair and a kit are also disclosed.

The present disclosure relates to an interference screw for creating an interference fit between a bone tunnel and tissue. The screw includes a threaded body having a proximal end, distal end, and thread extending around the threaded body between the proximal and distal ends. A supporting spline extends along a cannulation through the threaded body. The supporting spline is engagable with a delivery device. The screw further includes at least one opening defined by a surface between threads of the threaded body. A ratio of open surface area to closed surface area defines the opening and is selected such that, when torsionally loaded, the screw does not exhibit plastic deformation when inserted into an undersized bone tunnel. The screw further includes a tapered tip extending from the distal end of the threaded body. The tapered tip has a thread extending at least partway around the tapered tip.

A tendon repair implant and related surgical instruments are disclosed. The tendon repair implant has an elongated substrate with a convex side and a concave side with a plurality of spikes protruding from the concave side at an angle that optimally retains a. tendon to the bone that the tendon repair implant is subsequently attached to. A surgical retainer for the tendon repair implant is also provided that releasably retains the tendon repair implant during surgery and implantation, A drill guide instrument for the tendon repair implant Is also provided that allows the surgeon to precisely place fastening holes in the bone prior to implantation of the tendon repair implant.

A multiple drive interference screw device with a head having multiple insertion features. The screw component has a tubular body with a first end and a closed second end, and the head is positioned at the first end and configured to engage with a driver to advance the screw into the bone A penetrating tip is positioned at the second end. The head of the screw component has at least three insertion features, such as a hex shaped insertion feature around the major diameter of the head and a hexalobe shaped insertion feature within the hex shaped insertion feature, and a sprocket shaped insertion feature positioned exterior to the hex shaped insertion feature.

A dynamic ligament repair device includes a suture, a femoral side suture anchor and a threaded screw or housing implant. The screw is configured for placement in the tibia, or alternatively in the femur. A spring is housed inside an axial bore in the threaded screw. In some embodiments, the spring is a compression spring. A moveable spring button is positioned inside the axial bore adjacent a distal end of the spring. The spring button engages the spring directly in some embodiments. In alternative embodiments, an intermediate structure such as a spacer is positioned between the spring button and the spring. The suture extends between the spring button and the suture anchor. When the joint flexes or extends, the spring button travels inside the axial bore and dynamically compresses or relaxes the spring.

Devices, systems, implants and methods for achieving ligament fixation are disclosed. An implant includes a head member and an anchor member coupled to the head member. The implant includes tension member that couples the head member to the anchor member. The head member and the anchor member include a cannulation that receives the tension member therein. The implant may include a coupling member positioned between and coupling the head member and the anchor member, the coupling member including a cannulation that receives the tension member therethrough. Insertion instruments for inserting an implant for ligament fixation are also disclosed. Methods of using an implant for achieving ligament fixation are also disclosed.

Devices, systems and/or methods for repairing soft tissue adjacent a soft tissue repair site. In one embodiment, a repair device includes an anchor member, a capture member and one or more flexible members. The anchor member includes a base with at least four legs extending integrally from the base, the at least four legs configured to be moveable from a straight first position to a formed second position. The capture member is configured to be coupled to the anchor member such that the at least four legs of the anchor member move around structural portions of the capture member with the at least four legs of the anchor member in the formed second position. The one or more flexible members are coupled to the base of the anchor member, the one or more flexible members extending at least partially along the base of the anchor member.

A prosthesis to replace a flexor tendon pulley. The prosthesis comprises a tendon holding member with a hollow cylindrical shape and a connecting plate attached to the tendon holding member. The tendon holding member is configured to receive and hold a tendon of the human hand. The connecting plate is configured to be attached to a phalange of the human hand. The tendon holding member comprises an outer layer on an outer surface of the tendon holding member and an inner layer on an inner surface of the tendon holding member. The outer layer comprises hydroxyapatite to secure the tendon holding member to the surrounding tissues. The inner layer comprises of hyaluronic acid to secure the tendon holding member to the surrounding tissues.