A bone implant, particularly but not necessarily, for fixing bones of the foot is provided having body in the form of a crescent or arced shaped wedge, or a wedge in the shape of a crescent or arc. The crescent shaped wedge has bone screw bores that are each configured to hold a bone screw at a particular angle for receipt in a bone, eliminating the need to also use a plate. The crescent shape provides a graft area that allows introduction and retention of bone graft material to promote bone fusion. One or both tapered sides of the crescent shaped wedge may also have teeth, serrations or the like.

The disclosure is directed to a resilient implant for implantation into human or animal joints to act as a cushion allowing for renewed joint motion. The implant endures variable joint forces and cyclic loads while reducing pain and improving function after injury or disease to repair, reconstruct, and regenerate joint integrity. The implant is deployed in a prepared debrided joint space, secured to at least one of the joint bones and expanded in the space, molding to surrounding structures with sufficient stability to avoid extrusion or dislocation. The implant has opposing walls that move in varied directions, and an inner space filled with suitable filler to accommodate motions which mimic or approximate normal joint motion. The implant pads the damaged joint surfaces, restores cushioning immediately and may be employed to restore cartilage to normal by delivering regenerative cells.

An implant is provided for use in an ankle joint between reconditioned end surfaces established on a distal end of an upper tibia bone and an opposing lower talus bone. The implant comprises a substantially porous rigid component adapted to be anchored against the upper tibia reconditioned end surface and the lower talus reconditioned end surface. The component defining an opening therethrough. An intramedullary nail is configured to pass through the opening in the component when the nail is driven through the talus and into the tibia.

A bone implant, particularly but not necessarily, for fixing bones of the foot is provided having body in the form of a crescent or arced shaped wedge, or a wedge in the shape of a crescent or arc. The crescent shaped wedge has bone screw bores that are each configured to hold a bone screw at a particular angle for receipt in a bone, eliminating the need to also use a plate. The crescent shape provides a graft area that allows introduction and retention of bone graft material to promote bone fusion. One or both tapered sides of the crescent shaped wedge may also have teeth, serrations or the like.

One embodiment of the invention includes a sinus tarsi implant with a proximal portion that includes a spherical portion. The spherical portion may include apertures for tissue in-growth. The implant design limits patient discomfort due to pressure points. Other embodiments are disclosed.

A bone implant, particularly but not necessarily, for fixing bones of the foot is provided having body in the form of a crescent or arced shaped wedge, or a wedge in the shape of a crescent or arc. The crescent shaped wedge has bone screw bores that are each configured to hold a bone screw at a particular angle for receipt in a bone, eliminating the need to also use a plate. The crescent shape provides a graft area that allows introduction and retention of bone graft material to promote bone fusion. One or both tapered sides of the crescent shaped wedge may also have teeth, serrations or the like.

The disclosure is directed to a resilient implant for implantation into human or animal joints to act as a cushion allowing for renewed joint motion. The implant endures variable joint forces and cyclic loads while reducing pain and improving function after injury or disease to repair, reconstruct, and regenerate joint integrity. The implant is deployed in a prepared debrided joint space, secured to at least one of the joint bones and expanded in the space, molding to surrounding structures with sufficient stability to avoid extrusion or dislocation. The implant has opposing walls that move in varied directions, and an inner space filled with suitable filler to accommodate motions which mimic or approximate normal joint motion. The implant pads the damaged joint surfaces, restores cushioning immediately and may be employed to restore cartilage to normal by delivering regenerative cells.

A prosthesis including a magnetic implant approximating the size of a bone to be replaced; a first magnetic bone implant securable to a first bone adjacent the bone to be replaced; and a second magnetic bone implant securable to a second bone adjacent the bone to be replaced. Each of the first and second magnetic bone implants have a magnetic relationship with the magnetic implant. A method of reconstructing a wrist includes removing a patient's scaphoid to create a void. The scaphoid has a plurality of adjacent bones, each of the adjacent bones comprising a surface generally facing the void. The surface of at least two of the adjacent bones is prepared by affixing a magnetic element thereto and a magnetic scaphoid implant is inserted into the void. A magnetic relationship exists between the magnetic elements and the magnetic scaphoid implant.

A prosthesis including a magnetic implant approximating the size of a bone to be replaced; a first magnetic bone implant securable to a first bone adjacent the bone to be replaced; and a second magnetic bone implant securable to a second bone adjacent the bone to be replaced. Each of the first and second magnetic bone implants have a magnetic relationship with the magnetic implant. A method of reconstructing a wrist includes removing a patient's scaphoid to create a void. The scaphoid has a plurality of adjacent bones, each of the adjacent bones comprising a surface generally facing the void. The surface of at least two of the adjacent bones is prepared by affixing a magnetic element thereto and a magnetic scaphoid implant is inserted into the void. A magnetic relationship exists between the magnetic elements and the magnetic scaphoid implant.

An implant is provided for use in an ankle joint between reconditioned end surfaces established on a distal end of an upper tibia bone and an opposing lower talus bone. The implant comprises a substantially porous rigid component adapted to be anchored against the upper tibia reconditioned end surface and the lower talus reconditioned end surface. The component defining an opening therethrough. An intramedullary nail is configured to pass through the opening in the component when the nail is driven through the talus and into the tibia.