A fixation assembly for securing parts of a sternum is provided. The assembly comprises a flexible elongated member and an attachment member. The flexible elongated member includes a locking structure configured to secure the flexible elongated member in a loop around the sternum parts. The attachment member has at least one opening for receiving a bone fastener and is coupled to the flexible elongated member.

Disclosed is a bone repair system, in particular for treatment of fractures or defects of the pars interarticularis. In an embodiment, the bone repair system comprises a support member and a fastening member. The support member is configured to be fixed to a first bone or bone fragment. The fastening member includes a first and a second end portion and an elongate portion extending between the first and the second end portions. The first end portion is coupled to the support member, and the elongate portion is configured to loop around at least one second bone or bone fragment. The support member includes fixation means for adjustably securing the second end portion of the fastening member so as to stabilize and/or fix the first and the second bone or bone fragment with respect to each other.

Disclosed is a bone repair system, in particular for treatment of fractures or defects of the pars interarticularis. In an embodiment, the bone repair system comprises a support member and a fastening member. The support member is configured to be fixed to a first bone or bone fragment. The fastening member includes a first and a second end portion and an elongate portion extending between the first and the second end portions. The first end portion is coupled to the support member, and the elongate portion is configured to loop around at least one second bone or bone fragment. The support member includes fixation means for adjustably securing the second end portion of the fastening member so as to stabilize and/or fix the first and the second bone or bone fragment with respect to each other.

A new implant for bone fracture treatment that can easily and securely fix bone fragments is provided. An implant 2 for bone fracture treatment that covers bone fragments gathered at a site to be treated for a bone fracture in a living body and reduces and fixes the site invasively includes a metal knit portion 10 formed by knitting a metal string 11 constituted by one or a plurality of biocompatible metal string elements 12 into a cylindrical shape by circular knitting. The implant 2 further includes a resin knit portion 30 formed by knitting a resin string 31 constituted by one or a plurality of biocompatible resin string elements into a cylindrical shape by circular knitting. The metal knit portion 10 and the resin knit portion 30 are knitted to be continuous in an axial direction.

A neutralization plate includes a main body, a pair of upper arms extending upwards from the main body, and a pair of lower arms extending downward from the main body to form a generally X-shape with the pair of upper arms. In addition, the neutralization plate includes a horizontal channel formed across a rear side of a midsection of the main body, an aperture formed in the main body between the pair of lower arms and contiguous to a bottom edge of the horizontal channel, and a lower chute formed between the aperture and a lower edge of the horizontal channel. The lower chute is configured for ends of a suture looped through a fractured bone to be passed through the aperture and down the lower chute to a front side of the main body to be anchored separately from the fractured bone.

An anchor for anchoring tensile members to bone includes: a housing extending along a central axis, with a hollow interior; a collet in the hollow interior having a central bore for accepting tensile members and an exterior surface, the collet being configured to swage around and against tensile members; a sleeve having a peripheral wall defining interior and exterior surfaces, the sleeve disposed in the housing's hollow interior axially adjacent to the collet, and movable parallel to the central axis between first and second positions; and wherein at least one of the collet exterior surface and the sleeve interior surface is tapered and the sleeve and the collet are arranged so movement of the sleeve from the first position to the second position causes the sleeve interior surface to bear against the collet exterior surface, causing the collet to swage radially inwards around and against one or more tensile members.

An anchor for anchoring tensile members to bone includes: a housing extending along a central axis, with a hollow interior; a collet in the hollow interior having a central bore for accepting tensile members and an exterior surface, the collet being configured to swage around and against tensile members; a sleeve having a peripheral wall defining interior and exterior surfaces, the sleeve disposed in the housing's hollow interior axially adjacent to the collet, and movable parallel to the central axis between first and second positions; and wherein at least one of the collet exterior surface and the sleeve interior surface is tapered and the sleeve and the collet are arranged so movement of the sleeve from the first position to the second position causes the sleeve interior surface to bear against the collet exterior surface, causing the collet to swage radially inwards around and against one or more tensile members.

Devices and methods for placing an implant between two bone portions are disclosed. In some embodiments, a method comprises disposing a portion of a flexible member through a first bone portion, through an aperture in a trial implant, and through a second bone portion. The trial implant can be withdrawn to enable an implant to be coupled to the flexible member. The method includes applying tension to the flexible member to urge the implant into the space between two bone portions. In some embodiments, the two bone portions are facets.

Devices and methods for placing an implant between two bone portions are disclosed. In some embodiments, a method comprises disposing a portion of a flexible member through a first bone portion, through an aperture in a trial implant, and through a second bone portion. The trial implant can be withdrawn to enable an implant to be coupled to the flexible member. The method includes applying tension to the flexible member to urge the implant into the space between two bone portions. In some embodiments, the two bone portions are facets.

A joint stabilization (reduction) system and associated methods and tools for placement of the system in an open or minimally invasive technique. The joint stabilization system includes a flexible prosthetic band for stabilizing the bones in proper position and a connector mechanism for joining the two ends of the prosthetic band around the bones. One end of the prosthetic band can be permanently attached to the connector.