Implants for the fusion or fixation of two bone segments are described. For example, the implants can be used for the fusion or fixation of the sacroiliac joint. The implants can have a matrix structure, have a rectilinear cross-sectional area, and have a curvature.

An expandable intervertebral fusion cage is independently expandable vertically and laterally. The fusion cage includes a cage body that can receive an expansion member that causes the fusion cage to expand vertically. The cage body is responsive to a compressive force to move to an expanded lateral position, whereby the fusion cage defines a substantially circular annular profile.

Provided is a spinal implant having a unit structure printed by using a 3D printer, which is inserted between a vertebra and an adjacent vertebra and in which unit bodies constituted by at least one or more circular rings are repeated with a certain pattern. The spinal implant may implement elastic force like the existing vertebrae while bone fusion is performed as well as a state in which the bone fusion is completed after a procedure to obtain superior procedure results.

A medical product (100), preferably for use in treating, in particular filling and/or closing a bone cavity, wherein the product (100) comprises a plurality of interconnected members (110), wherein each member (110) has a peripheral boundary (120) and the boundaries (120) of adjacent members (110) engage with one another. Also, a method for producing the medical product (100) and a medical kit that comprises the medical product (100) and a securing element for securing the product (100) in a bone cavity and to a method for filling a bone cavity.

Shoulder arthroplasty systems and configurations for components thereof are described. For example, implant systems for a total should arthroplasty (TSA), hemi shoulder arthroplasty, and reverse should arthroplasty (RSA) are described. In addition, exemplary configurations for baseplates, glenoid components, glenosphere components, humeral components, humeral head components, humerosocket components, connectors, and adaptors, are described.

Described herein is a bone implant including at least one bone-engaging surface designed to mate with an implant-engaging surface of a bone. In the preferred embodiment, the bone-engaging surface of the implant includes a wave pattern comprising at least one peak extending in a proximal direction or at least one valley extending in a distal direction. The implant-engaging surface of the bone also includes a matching wave pattern having at least one peak and valley. Upon mating the engaging surfaces, a bone-implant interface may be created wherein the peaks and valleys of the wave patterns are aligned. As a result, there is good surface contact area at the bone-implant interface which helps prevent loosening or rotating of the implant.

Shoulder arthroplasty systems and configurations for components thereof are described. For example, implant systems for a total should arthroplasty (TSA), hemi shoulder arthroplasty, and reverse should arthroplasty (RSA) are described. In addition, exemplary configurations for baseplates, glenoid components, glenosphere components, humeral components, humeral head components, humerosocket components, connectors, and adaptors, are described.

A placeholder for vertebrae or vertebral discs includes a tubular body, which along its jacket surface has a plurality of breakthroughs or openings for over-growth with adjacent tissue. The placeholder includes at least a second tubular body provided with a plurality of breakthroughs and openings at least partially inside the first tubular body. The first and second tubular bodies can have different cross-sectional shapes, can be are arranged inside one another by press fit or force fit or can be connected to each other via connecting pins and arranged side by side to one another in the first body.

A cranial plate is provided for use after a craniectomy. The plate is mounted to the skull and protects the brain exposed in the skull opening. A plate is initially spaced above the skull with gaskets or spacers so as to preclude pressure on the brain. The gaskets or spacers are resorptive, or otherwise dissolve or shrink over time, until the plate settles upon the skull. An elastic web extending over the plate provides a constant force to pull the plate towards the skull as the spacers shrink. The plate is secured to the skull using screws. The plate may include alignment posts residing adjacent the skull opening to maintain proper positioning of the plate as the spacers shrink. The plate eliminates the need for a second cranioplasty surgical procedure.

For the purpose of providing a flexible implant in a plane direction which prevents a scalp from sinking into an osteotomy line after surgery when joining or reconstructing the bone, implant 1 used for bone joining or reconstruction includes base units 11. The base unit 11 includes a first annular ring 10, a second annular ring 20 positioned opposite the first annular ring, and a first connecting portion 41 connecting the first annular ring 10 and the second annular ring 20. The basic units 11 are linearly linked by a second connecting portion 42 such that a first annular ring row 101 formed by a plurality of the first annular rings 10 and a second annular ring row 201 formed by a plurality of the second annular rings 20 are in parallel, and the basic units form a mesh that is capable of meandering along an osteotomy line.