Illustrative embodiments of orthopedic implants and methods for surgically repairing hammertoe are disclosed. According to at least one illustrative embodiment, an orthopedic implant includes a proximal segment comprising a number of spring arms forming an anchored barb at a first end of the implant, a distal segment extending between the proximal segment and a second end of the implant, and a central segment disposed between the proximal and distal segment.

This interphalangeal arthrodesis implant comprises a proximal anchor portion intended to be engaged and anchored in the medullary canal of a first phalanx sectioned along a first osteotomy plane, the proximal anchor portion including a plurality of proximal anchor branches each provided with at least one bone anchor element; and a distal anchor portion, connected to the proximal anchor portion, intended to be engaged and anchored in the medullary canal of a second phalanx sectioned along a second osteotomy plane, the distal anchor portion including a plurality of distal anchor branches each provided with at least one bone anchor element. The distal anchor portion comprises a stop portion including a stop surface intended to bear against a sectioned surface of the first phalanx extending along the first osteotomy plane.

An orthopedic implant includes a porous insert having a first insert portion having a first insert thickness and a second insert portion having a second insert thickness. The implant includes a non-metallic structure having a first non-metallic portion having a first non-metallic thickness and a second non-metallic portion having a second non-metallic thickness. The first non-metallic portion is attached to the first insert portion and the second non-metallic portion is attached to the second insert portion. Either or both of the second insert thickness being different from the first insert thickness and the second non-metallic thickness being different from the first non-metallic thickness. The porous insert includes a porous projection extending into the non-metallic structure.

A bone implant comprising an elongate body having a first end and a second end coupled by a shaft is disclosed. The first portion is configured to couple to a first bone. The second portion comprises a first expandable section comprising at least one expandable feature. The first expandable section is configured to be received within a reverse countersink in a second bone in a collapsed state and to expand within the reverse countersink. The expandable feature couples to a bearing surface of the reverse countersink. A surgical tool comprising a shaft and at least one expandable cutting edge is disclosed. The shaft is sized and configured to be received within a canal formed in a bone. The expandable cutting edge is formed integrally with the shaft. The expandable cutting edge is configured to expand from a collapsed position to an expanded position for forming a reverse countersink.

A pin made of cortical bone may be inserted into adjoining bones of a toe to align and secure the bones. The pin may have barbs to prevent migration of the pin. The pin may include a shoulder to further prevent migration of the pin from the bones, to increase the strength of the pin, and to increase the surface area between the bone pin and the host bone. The pin may further include flattened portions on its circumference to aide in rotating the pin during insertion. The pin may be treated to reduce brittleness.

A device for repairing Hallux Valgus (HV) is disclosed comprising a first arm adapted to be affixed inside the canal of the first metatarsus (1MT) of a human foot, a second arm adapted to be affixed inside the canal of the second metatarsus (2MT) of a human foot and a spring mechanism connected between the first arm and the second arm, active to push the 1MT closer to the 2MT. The device may comprise fixating means adapted to fixate said first arm inside said MT and said second arm inside said 2MT and the spring mechanism is removable from the first and the second arms.

A subtalar joint prosthesis that is adapted to replace the natural subtalar joint that exists between a patient's talus and calcaneus bones includes talar and calcaneal components. Each of these is configured to have a shape that is herein defined as being a portion of the boundary surface of a frustum. Meanwhile, these components' inner surfaces are configured to: (a) generally follow the anatomic contour of the original joint surface to which each component is to be attached, and (b) minimize each components's average thickness, consistent with providing sufficient strength and rigidity for the components, so as to require minimum bone resection for the implantation of these components.

The invention concerns an arthrodesis implant (1) allowing promoting the bone fusion of two bones, said implant (1) comprising: a rigid and non-deformable anchoring body (4), designed to ensure the anchoring of the implant (1) in a first bone (2), a deformable portion (5) designed to ensure the anchoring of the implant (1) in a second bone, said deformable portion (5) comprising at least two anchoring arms (9, 10) which protrude beyond the anchoring body (4) from the base end (7) of the latter, the anchoring arms (9, 10) being separated from each other by a free space (E) so as to be able to be brought closer to each other by deformation of said anchoring arms under the action of the second bone. and being characterized in that at least one of the anchoring arms (9, 10) is provided with a longitudinal reinforcing fin protruding beyond the anchoring arm (9, 10) from a lateral side (20) of the latter. Osteosynthesis surgical implants.

An implant can be used for the treatment of fat pad atrophy. The implant can be installed in the ball of the foot, the heel of the foot, the hands, or other areas. The implant can supplement or replace a patient's fat pads. In some instances, the implant can include an implant pad having a non-permeable external lining and an internal cavity enclosed by the external lining. The internal cavity can include a filler material. The implant can include features that resist rupture and/or migration.

An implant or endoprosthesis suitable to be implanted in human or animal tissue includes two (or more than two) parts to be joined in situ. Each one of the parts includes a joining location, the two joining locations facing each other when the device parts are positioned for being joined together, wherein one of the joining locations includes a material which is liquefiable by mechanical vibration and the other one of the joining locations includes a material which is not liquefiable by mechanical vibration and a structure (e.g. undercut cavities or protrusions) suitable for forming a positive fit connection with the liquefiable material. The joining process is effected by pressing the two device parts against each other and by applying ultrasonic vibration to one of the device parts when the two parts are positioned relative to each other such that the two joining locations are in contact with each other.