The invention describes an implant for wear couples in endoprosthetics, comprising at least one shell, into which an insert, preferably a ceramic insert, is introduced. The insert has an outer side, with an outer face, and an inner side, and a hemispherical wear region for accommodating a spherical wear partner being formed on the inner side. The aim of the invention is to reduce the height of the implant as much as possible and to ensure that, e.g., the pelvic bone does not have to be milled down as much. According to the invention, the insert is therefore designed in the form of a ring or annular structure. In order to reduce friction between the spherical wear partner and the implant to a minimum, the implant has a specially designed inner geometry.

There is disclosed a bone fixation device that can include a cage having an optional mesh portion. The bone fixation device can be configured to couple a leg portion to a foot portion of a user's body. In at least one embodiment, the device includes at least one cage having a plurality of struts forming cells. There can be an optional mesh portion having a pre-set porosity that can be either constant or variable in density. In at least one embodiment there can be a cage portion which is substantially spherical shaped. Alternatively, the device can be substantially egg shaped. In at least one embodiment there can be a central post hole for receiving a post. In another embodiment at least one plate or shaft can connect to the cage.

An expandable wedge implant for wedge osteotomies of the extremities has first and second components which are pivotally attached to each other such that up and down pivoting of the two components relative to one another causes increase and decrease of implant height. A pivot control structure is operably coupled to and between the two components to effect pivoting. Linear movement of a threaded ball on a threaded shaft associated with the first component while the threaded ball is concurrently constrained within an angled channel of the second component causes pivoting of the second component relative to the first component. Anchoring members associated with the first and second components attach the implant to adjacent vertebral bodies.

A system can include a plurality of grouter devices configured to lodge in one or more focal defects located on a pair of articular surfaces; and a plurality of buffer devices configured to fill a space between the pair of articular surfaces; wherein the plurality of grouter devices and the plurality of buffer devices are sized and shaped such that a contact pressure between the pair of articular surfaces is diminished.

Devices and methods of correcting vertebral misalignment, including, e.g., spondylolisthesis, are disclosed. In one embodiment, a vertebral implant may include an assembly configured to be secured to a first vertebral body, wherein the assembly includes a frame made of a first material and at least one end plate made of a second material different than the first material; a reducing plate configured to be slidably received over the central portion, wherein the reducing plate is configured to be secured to a second vertebral body; and an actuator configured to move the reducing plate relative to the frame.

A glenoid implant is provided and may include a body portion and a stem portion. The stem portion may extend from the body portion along a longitudinal axis. The body portion may include an articular side and a bone-engaging side opposite the articular side. At least a portion of the bone-engaging side may be disposed at a non-parallel angle relative to at least a peripheral edge of the articulation side.

A prosthetic ankle includes a tibial portion likely to be connected to the lower end of a tibia, a talus portion likely to be connected to a talus, and a pad inserted between the tibial portion and the talus portion. The tibial portion includes an articular surface likely to engage with a contact surface of the pad. The talus portion includes a curved articular surface likely to engage with a contact surface of the pad. The articular surface of the tibial portion is curved, concave and includes a flat section forming an extension to the rear of said articular surface.

A method for treating a spine includes the steps of: creating a surgical pathway in a body along a first surgical approach to a surgical site including vertebral tissue; creating a surgical pathway in the body along a second surgical approach to the surgical site including the vertebral tissue; disposing a fulcrum with an intervertebral disc space of the vertebral tissue via the first surgical approach; and manipulating the vertebral tissue via the second surgical approach. Spinal implants, surgical instruments and systems are disclosed.

The present invention relates to pliable, compression-resistant bone-based products and methods of making the same.

A surface-reconfiguration implant, a method of using the surface-reconfiguration implant, and a method of implantation of the surface-reconfiguration implant that creates an articular surface between an upper portion of a humeral head and a greater tuberosity, and an undersurface of an acromion in shoulders with massive rotator cuff tears is provided. The surface-reconfiguration implant can include a body portion including at least an undersurface and an articular surface, where the undersurface is configured to interface with portions of a proximal humerus to facilitate attachment of the body portion thereto, and portions of the articular surface extend to and/and preferably beyond a normal anatomical shape of portions a humeral head and a greater tuberosity both superiorly and medially when the body portion is attached to the proximal humerus.