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.

Stand-alone interbody fusion devices for engagement between adjacent vertebrae. The stand-alone interbody fusion devices may include frames and one or more endplates coupled to the frame. The frame may be configured and designed to provide the apertures which are designed to retain bone fasteners, such as screws or anchors, and secure the implant to the adjacent vertebrae.

A method of inserting a screw into a fusion cage, comprising the step of: i) attaching a screw head of a bone screw to a flexible bone screw driver comprising: a) a proximal handle, b) an intermediate shaft, c) a flexible distal end portion comprising a plurality of interlocking segments portion defining a periphery and a distal tip adapted to engage the screw head, and d) a flexible pre-bent sleeve that is configured to be placed radially over and around the plurality of interlocking segments to provide a loaded configuration,
wherein the plurality of interlocking segments portion is substantially straight in its unloaded configuration,
whereby the pre-bent sleeve pre-determines the trajectory of the tip in the loaded configuration, ii) inserting the bone screw into a threaded throughhole of a fusion cage comprising a front wall, a pair of opposing side walls, a back wall, and top and bottom surfaces adapted for gripping opposed vertebral endplates, wherein the front wall comprises the threaded throughhole.

A method of manufacturing an implant, including mixing a first quantity of biocompatible polymer particles, a second quantity of bioactive ceramic particles, and a third quantity of fugitive material particles to define an admixture, forming the admixture to define a composite body having an inferior portion, a superior portion and a central portion disposed between the inferior and superior portions, heating the admixture to fuse the first quantity of bioactive polymer particles to define a composite implant body, and infiltrating the composite implant body with a solvent to remove fugitive material particles to yield a network of interconnected pores and to define a porous implant body. The fugitive material particles are hollow spheres partially filled with a material selected from the group comprising air, bioactive agents, biological growth enhancers, drugs, and biocompatible polymer material, combinations thereof.

An MTS medial tibial plateau patch, a modular MTS medial tibial plateau patch, and a minimally invasive replacement method thereof are disclosed. The MTS medial tibial plateau patch includes an articular surface provided with an arc-shaped recessed area and a bottom surface provided with 3 stand columns distributed triangularly, or two longitudinal keels having non-parallel distribution or two triangular keel wings, and the arc-shaped recessed area is well matched and in a sliding fit with a femoral condyle without an increase in impact in a joint, thus guaranteeing a stability of a prosthesis, realizing a concept of a minimally invasive surgery, and reducing damage to a normal tissue. The modular MTS medial tibial plateau patch includes a bone-trabecula metal tibial support and a liner made of VE high cross-linked polyethylene.

An intervertebral implant for implantation in an intervertebral space between vertebrae. The implant includes a body having a front end, a rear end and a pair of spaced apart first and second side walls extending between the front and rear ends. The front and rear ends extend in a transverse direction and a central axis of the body extends from the rear end to the front end. The rear end defines a first fastener hole having a first central axis and a second fastener hole having a second central axis. The first and second central axes extend parallel to one another at an acute angle relative to the body central axis in the transverse direction.

A system for replacing a portion of an articular surface including providing an implant site and installing an implant into the implant site. The implant site includes a first and a second excision site which at least partially intersect with one another. Each of the first and second excision sites are formed by providing a respective axis and excising a portion of the articular surface relative to the respective axes.

A robotic system for preparing a bone to repair a bone fracture, includes a controllable guide structure configured to guide preparation of at least one bone piece during execution of a surgical plan and a control system configured to define the surgical plan. Defining the surgical plan includes determining a desired relationship between at least a first bone piece and a second bone piece that are separated by the bone fracture and planning preparation of the first bone piece to include a prepared anatomical structure configured to align the first bone piece with the second bone piece such that when aligned, the first bone piece and the second bone piece will achieve the desired relationship. The control system is further configured to control the controllable guide structure according to the surgical plan.

A robotic system for preparing a bone to repair a bone fracture, includes a controllable guide structure configured to guide preparation of at least one bone piece during execution of a surgical plan and a control system configured to define the surgical plan. Defining the surgical plan includes determining a desired relationship between at least a first bone piece and a second bone piece that are separated by the bone fracture and planning preparation of the first bone piece to include a prepared anatomical structure configured to align the first bone piece with the second bone piece such that when aligned, the first bone piece and the second bone piece will achieve the desired relationship. The control system is further configured to control the controllable guide structure according to the surgical plan.

The invention relates to a glenoid (shoulder socket) implant prosthesis, a humeral implant prosthesis, devices for implanting glenoid and humeral implant prostheses, and less invasive methods of their use for the treatment of an injured or damaged shoulder.