An artificial intervertebral disc (IVD) is provided for replacement of a degenerated intervertebral disc. The artificial IVD includes two endplates having oppositely-facing outward surfaces configured to engage respective intervertebral surfaces of the spinal column, and a chamber, which is disposed between oppositely-facing inner surfaces of the two endplates, and which includes a lateral wall including an electroosmotic membrane. A plurality of exposed electrode surface includes (i) one or more intra-chamber exposed electrode surfaces, which are located within the chamber; and (ii) one or more extra-chamber exposed electrode surfaces, which are located outside the chamber, in a vicinity of the chamber. Control circuitry is configured to drive at least one of the one or more intra-chamber exposed electrode surfaces and at least one of the one or more extra-chamber exposed electrode surfaces to electroosmotically drive liquid from outside the chamber to inside the chamber. Other embodiments are also described.

A trumpet expandable vertebral device, includes: a center shaft having a front end and a rear end; a trumpet expandable part mounted outside and surrounding the center shaft, wherein the trumpet expandable part includes: plural expandable plates, each expandable plate having a thickness which increases from the front end toward the rear end; a fixed part, for fixing the relative position of the trumpet expandable part with respect to the center shaft in an axial direction of the center shaft, but allowing the center shaft to rotate with respect to the trumpet expandable part within the fixed part in a radial direction of the center shaft; and a connection part for connecting the trumpet expandable plates with the fixed part; a trumpet expanding ring mounted outside and surrounding the center shaft, wherein the trumpet expanding ring is located between the center shaft and the trumpet expandable part in the radial direction; wherein when the trumpet expanding ring moves toward the rear end relatively to the trumpet expandable part, the trumpet expandable plates are expanded to expand a vertebra.

The present invention relates generally to a prosthetic spinal disc for replacing a damaged disc between two vertebrae of a spine and methods for inserting said discs. The intervertebral prosthetic discs are provided with connections for facilitating implantation and removal and features which enhance primary and secondary stability over time.

The device for maintaining an intervertebral space is capable of being accommodated inside the disc, in place of the core. Natural anchoring is ensured by promoting the regrowth of fibre around at least part of the device. The possibility of ejection of the residual core is limited in order to avoid a renewed hernia, and mobility of the vertebral column is ensured. To this end, a subject of the invention is a device having at least two non-expansible concentric rings which between them form a free space and which are connected to each other via two junction summits.

A bone stabilization plate system. The bone stabilization plate system includes a base plate configured to fit primarily between an anterior portion of a first bone's lip osteophyte and an anterior portion of a second, adjacent bone's lip osteophyte. The bone stabilization plate system includes a plurality of bone screws configured to fit in respective bone screw holes in the base plate to secure the base plate.

The present invention relates to a safety element, an implant comprising such a safety element and an implant system comprising an implant with the safety element. The safety element for an implant is arranged between an outer and inner part of an implant, wherein the safety element engages into the gearing of an expansion ring, wherein a releasing space between outer part and inner part of the implant is provided into that the safety element is to be radially moved for enabling rotation of the expansion ring.

The present invention relates to a system and method for spinal disc replacement surgery via a lateral approach. The invention also relates to a spinal disc replacement device that is designed to be inserted via the lateral approach disc replacement surgery. The invention further relates to tools used for the spinal disc replacement surgery via the lateral approach.

A selection system comprises a ring, a plurality of shims, a measurement device, and at least one glenoid component. The ring is configured to couple to a humerus. A shim of the plurality of shims is configured to couple to the ring. The measurement device is configured to couple to the shim. Each shim of the plurality of shims has a different height when coupled to the ring. The selection system generates measurement data to support the selection of at least one prosthetic component for a shoulder joint in a surgical environment. The shoulder joint geometry can be adjusted by changing shims, changing glenoid component or both. The selection system is removed after the selection of the final prosthetic components for the shoulder joint. The final prosthetic components are installed in the shoulder joint. The measurement device is placed in the shoulder joint and measurement data is generated to verify performance.

A prosthesis for implantation in a de-nucleated intervertebral disc includes a fiber ring-like layer which encloses a polymeric layer to create an annular space. The annular space is inflatable with an in-situ curable liquid polymer and forms an interior cavity. The annular space may be expanded uniformly or differentially to be tailored to the needs of a particular vertebral segment and to achieve optimal disc space width and angle, thereby stabilizing the segment while preserving normal motion of the vertebral segment. The interior cavity provides a void that allows inward deformation of the implant during weight bearing activities and bending. The prosthesis can be elastically deformed through axial elongation to a reduced profile to load into a delivery cannula using pulling techniques.

A medical device for treating hip joint osteoarthritis by providing a joint surface is provided. The medical device has at least two artificial hip joint surface parts adapted to be connected to each other to form an artificial hip joint surface during an operation. A method of treating a hip joint of a human patient by providing the medical device is also provided. The method includes cutting the skin of the human patient, dissecting an area of the pelvic bone on the opposite side from the acetabulum, creating a hole in the dissected area passing through the pelvic bone and into said hip joint and providing the medical device to the hip joint, through the hole in the pelvic.