An implant for filling a bore hole in a bone includes: a biocompatible plate having upper and lower surfaces; and a support frame having a central portion located at least partially within the plate, an outer rim having a plurality of fastening points adapted for attaching the implant to bone surrounding a bore hole in which the plate is inserted, and a plurality of arms extending between the central portion and the outer rim.

An expandable vertebral device with triangular connection beam includes: a rotatable center shaft; a fixed part, wherein the rotatable center shaft penetrates through the fixed part and is rotatable relative to the fixed part; a movable slide, surrounding a portion of the rotatable center shaft, and is movable along an axial direction of the rotatable center shaft in response to a rotation of the rotatable center shaft; at least one first connection beam, which is rotatably connected to the fixed part; at least one second connection beam, which is rotatably connected to the movable slide, and is rotatably connected to the corresponding first connection beam; whereby when the rotatable center shaft rotates within the fixed part so that the movable slide moves away from the fixed part, the first and second connection beams are expanded to restore a vertebra to its original shape.

This invention related to a method of forming a polymer component and comprises blending polymer particles with antioxidant to form a mixture in which the antioxidant coats the polymer particles, irradiating the polymer particles to cross-link the polymer particles therein and forming the irradiated mixture into a consolidated component. The invention also relates to a method of forming an articular surface for a prosthesis and a prosthesis having a polymer articular bearing surface wherein at least one predetermined portion of the bearing surface is provided with cross-linked polymer bonds.

In embodiments of the invention, an implant that anchors into bone may have a bone-facing region that comprises a plurality of interconnected struts. The interconnected struts may define local features such as engagement ridges, fins, crests, a macroscopic surface-interrupting feature, a divertor structure, and sawteeth in any combination. Such features may help resist translation or rotation of the implant, and may be conducive to bone ingrowth. Parameters such as local empty volume fraction and local average strut length can be varied, even within the features, by the design of the network of struts. Struts may be tapered. Cantilever struts may also be provided, which may point in a desired direction. The pattern of struts may be specified to the level of dimensions and location of individual struts. The implant may be manufactured by additive manufacturing methods. The mesh of struts may be generated by an algorithm using Voronoi tessellation.

A joint implant for temporary or permanent use has a femoral component and tibial component. The femoral component has a base and rod extending therefrom and defines a pin. The tibial component has a base and rod extending therefrom and defines a bore in which the pin is seated so that the femoral component is rotatable relative to the tibial component.

A spinal bone graft includes one or more cortical bone portions forming a first unit. The first unit includes an engagement surface for contacting bone, and a mating surface. The mating surface forms at least one first undercut. The bone graft also includes one or more cortical bone portions forming a second unit. The second unit includes an engagement surface for contacting bone, and a mating surface. The mating surface forms either at least one second undercut, or at least one connector. In the former, at least one connector is received in each of the first and second undercuts to interconnect the first and second units. In the latter, the at least one connector of the second unit is received in the first undercut of the first unit to interconnect the first unit and second unit.

The embodiments provide various interbody fusion spacers, or cages, for insertion between adjacent vertebrae. The cages may have integrated expansion and angular adjustment mechanisms that allow the cage to change its height and angle as needed, with little effort. The cages may have a first, insertion configuration characterized by a reduced size to facilitate insertion through a narrow access passage and into the intervertebral space. The cages may be inserted in a first, reduced size and then expanded to a second, larger size once implanted. In their second configuration, the cages are able to maintain the proper disc height and stabilize the spine by restoring sagittal balance and alignment. Additionally, the intervertebral cages are configured to be able to adjust the angle of lordosis, and can accommodate larger lordotic angles in their second, expanded configuration. Further, these cages may promote fusion to further enhance spine stability by immobilizing the adjacent vertebral bodies.

A spacer system replaces or substitutes for a medical implant in a patient. The system includes a housing comprising a shape similar to the medical implant; an aperture in the housing, a subcutaneous port configured to receive a medicament, the subcutaneous port being in fluid communication with the aperture; and at least one channel within the housing, wherein the at least one channel extends from the aperture to an exterior surface of the housing to equally distribute a material the medicament from the aperture through the at least one channel. The subcutaneous port is in fluid communication with the aperture through a catheter connecting the subcutaneous port to the aperture. The system may be used to replace a variety of medical implants, including a hip implant, an intramedullary nail, a pedicle screw, a knee implant, a sternum prosthesis, and a clavicle prosthesis, an ankle implant, shoulder implant, tibia implant, femur implant, humerus implant, spinal cage, external fixation pin, intercalary fusion device, talus implant, or a vertebral body implant.

Embodiments of an implant for use in surgery are disclosed. The implant may include elastic polymer file made from a suitable biologically compatible polymer. The implant may also include a reinforcement element.

A joint replacement system for repairing an articular surface of a first bone of a joint includes an anchor portion and an implant portion. The anchor portion includes an anchor to be secured to the bone, and an anchor fixation head including a bone-facing surface (BFS) extending radially outward from the anchor and an implant facing surface (IFS) extending from a periphery of the BFS. The implant portion is formed from a material (e.g., CoCr) more dense than the material of the anchor portion (e.g., Ti) and includes a fixation cavity to receive at least a portion of the anchor fixation head (AFH), the fixation cavity includes an anchor facing surface (AFS) configured to form a frictional connection with the IFS, and a load bearing surface having a contour for articulating against a cooperating articulating surface of a second bone of the joint.