A medical implant for cartilage and/or bone repair at an articulating surface of a joint includes a contoured implant body and at least one extending post. The implant body has an articulating surface configured to face the articulating part of the joint and a bone contact surface configured to face the bone structure of a joint, where the articulating and bone contact surfaces face mutually opposite directions and the bone contact surface is provided with the extending post. A cartilage contact surface connects the articulating and the bone contact surfaces and is configured to contact the cartilage surrounding the implant body in a joint. The articulating surface has a layer that is a wear-resistant material. The cartilage contact surface has a coating that is a bioactive material.

The present invention provides a joint implant component as well as a method for the implantation thereof. The joint implant component (1), in particular of a hip endoprosthesis, has a proximal joint section (10), a distal anchoring section (30) and a transition section (20) having a fixation structure (21) between the joint section (10) and the anchoring section (30), the fixation structure being arranged in at least one part of the perimeter of the transition section (20) as an elongate recess (22) for guiding suture material.

An expandable interbody device for placement between adjacent vertebrae having an upper structure, a lower structure and a screw mechanism, wherein actuation of the screw mechanism moves the upper and lower structures between a collapsed configuration and an expanded configuration. A deployment tool couples to the expandable interbody device for positioning the device between adjacent vertebrae, actuating the screw mechanism and delivering a material to a chamber of the expandable interbody device.

An interspinous stabilizer, comprising: an interspinous spacer, comprising a central support, having a first direction and a second direction opposite to each other, and an upper side and a lower side perpendicular to the first direction and the second direction; an upper side wing is on the first direction and extending from the upper side of the central support; a lower side wing is on the first direction and extending from the lower side of the central support; an upper protrusion is on the second direction and extending from the upper side of the central support; a lower protrusion is on the second direction and extending from the lower side of the central support; at least one perforation, the perforation traversing through the first direction to the second direction of the central support.

Disclosed is a cervical plate having a polyester staple fiber laminated within a polycarbonate urethane. The polyurethane provides a flexible, high resilience structure with a Dacron material providing a flexible skeleton. The result is a cervical plate that is flexible but provides the necessary rigidity. An inflatable balloon can be used to mimic the properties of the natural disc by maintaining the intervertebral disc space through a full range of natural motion.

A tibial support of an artificial knee joint, comprising a main tibial support body and a tibial support platform, wherein the main tibial support body is wing-shaped, a central axis thereof being vertical to the tibial support platform. A plurality of hollow screw holes is provided at the upper part of the main body. The tibial support platform is located above the main tibial support body. The surface of the tibial support platform is an organic polymer material layer matching a tibial liner. The hollow screw holes in the tibial support are sealed by the polymer material layer. Because a tibial support of an artificial knee joint adopts a high-biocompatibility organic polymer material, physical machining is allowed in an operation, and meanwhile, the surface corrosion of the tibial support is reduced. Hollow screw holes are sealed by means of a polymer material layer, thereby inhibiting joint liquid from entering the holes, and reducing the transportation of particles. Recesses are provided at positions, corresponding to the screw holes, on the polymer surface, thereby aiding in drilling holes and mounting screws in an operation.

Various embodiments comprise an expansible intervertebral implant intended to be implanted in a space between two adjacent vertebrae to at least partly supplant an intervertebral disc, said implant being able to expand along three substantially mutually orthogonal axes so as to comply with the lordosis of the patient while still having increased stability and reliability.

An expansible intervertebral implant is disclosed, various embodiments of which comprise an elongated body along a longitudinal axis comprised between a proximal end and a distal end, a flexible arm mounted in the vicinity of the distal end of the longitudinal body and movable between: a folded-back position with the arm substantially parallel to the axis, and a deployed position with the arm not parallel to the axis and away from the body to expand said implant along an axis, by assuming the general shape of a circular arc, a means for deployment of said flexible arm for deploying the latter from the folded-back position to the deployed position, by the sliding of a proximal portion of said flexible arm with respect to the body inducing an increase in the space occupied by the implant, greater than the space of the implant in the folded-back position.

Resorbable implants, coverings and receptacles comprising poly(butylene succinate) and copolymers thereof have been developed. The implants are preferably sterilized, and contain less than 20 endotoxin units per device as determined by the limulus amebocyte lysate (LAL) assay, and are particularly suitable for use in procedures where prolonged strength retention is necessary, and can include one or more bioactive agents. The implants may be made from fibers and meshes of poly(butylene succinate) and copolymers thereof, or by 3d printing molding, pultrusion or other melt or solvent processing method. The implants, or the fibers preset therein, may be oriented. These coverings and receptacles may be used to hold, or partially/fully cover, devices such as pacemakers and neurostimulators. The coverings, receptacles and implants described herein, may be made from meshes, webs, lattices, non-wovens, films, fibers, foams, molded, pultruded, machined and 3D printed forms.

A bone implant includes at least one bone-engaging surface designed to mate with an implant-engaging surface of a bone. In the preferred embodiment, the bone-engaging surface of the implant includes a wave pattern comprising at least one peak extending in a proximal direction or at least one valley extending in a distal direction. The implant-engaging surface of the bone also includes a matching wave pattern having at least one peak and valley. Upon mating the engaging surfaces, a bone-implant interface may be created wherein the peaks and valleys of the wave patterns are aligned. As a result, there is good surface contact area at the bone-implant interface which helps prevent loosening or rotating of the implant.