An augment device for a joint endoprosthesis, the device including a sleeve surrounding a channel extending through the sleeve. The sleeve is formed of porous material for ingrowth of bony material, the sleeve comprising an inner face and an outer face. The sleeve further comprises a wall surrounding the channel, the wall being made of solid material and forming a sandwich structure with the porous material, wherein the wall forms a bulkhead between the inner face and the outer face. Thereby, the bulkhead wall will stop inflow of any cement across the sleeve from its inner to its outer face. The porous material on the outer face will be kept free from cement and its capability to promote bone ingrowth is reliably preserved. The augment devices are preferably provided as a set having different sizes and straight or stepped bottoms for improved versatility and maximum preservation of natural bone matter.

A system for tracking relative displacement between a first element and a second element in a structure, the system includes: a permanent magnet fixed relative to the first element; a magnetic sensor fixed relative to the second element, the magnetic sensor configured to measure a magnetic field strength; and a processor configured to determine the relative displacement between the first element and the second element, based on the magnetic field strength measured by the magnetic sensor. This invention has particular applications in e.g. orthopaedic prostheses. A related method includes the steps of measuring, using the magnetic sensor, a magnetic field strength; and determining the relative displacement between the relative displacement between the first element and the second element, based on the magnetic field strength measured by the magnetic sensor.

An augment device for a joint endoprosthesis, the device including a sleeve surrounding a channel extending through the sleeve. The sleeve is formed of porous material for ingrowth of bony material, the sleeve comprising an inner face and an outer face. The sleeve further comprises a wall surrounding the channel, the wall being made of solid material and forming a sandwich structure with the porous material, wherein the wall forms a bulkhead between the inner face and the outer face. Thereby, the bulkhead wall will stop inflow of any cement across the sleeve from its inner to its outer face. The porous material on the outer face will be kept free from cement and its capability to promote bone ingrowth is reliably preserved. The augment devices are preferably provided as a set having different sizes and straight or stepped bottoms for improved versatility and maximum preservation of natural bone matter.

Systems, devices and methods for providing orthopedic augments having recessed pockets that receive a fixation material. The orthopedic augments include an outer surface that interfaces with a patient's tissue or bone, an inner surface that interfaces with an implant and having a recessed pocket configured to receive a fixation material, a rim around at least a portion of the recessed pocket, and a port in the rim, wherein the recessed pocket extends along the inner surface in at least a lateral direction from the port.

One aspect relates to a seal for sealing a bone canal opening during the application of bone cement into the cancellous bone of a bone canal. The aspect also relates to a device for applying bone cement into the cancellous bone of a bone canal including the seal according to one embodiment, and a method for applying bone cement by using the device according to the embodiment.

An intervertebral spacing implant, including: a seat having an interior surface and an exterior surface; branches having an anterior end and a posterior end, the anterior end of the branches coupled to the seat and extending in a direction away from the seat, each of the branches having an interior surface and an exterior surface opposite the interior surface, the seat and the branches forming a cage, the exterior surface of the seat and the exterior surface of the branches defining an internal volume of the cage, the cage including fenestrations; a spacer configured to fit within the cage and move in the direction away from the seat and toward the posterior end of the plurality of branches, the spacer and the cage configured such that the branches will move from an unexpanded position to an expanded position when the spacer is urged in the direction away from the seat.

The present disclosure provides a device and method for applying a bone graft material to the body. The device includes a cylinder into which bone graft material is loaded. Specifically, the bone graft material is loaded into the cylinder through a funnel at a proximal end of the cylinder and dispensed through a tip at a distal end of the cylinder. After the bone graft material is loaded, a sleeve within the cylinder can be removed in order to create a channel within the bone graft material. Water or other hydrating fluid may be inserted into the channel through a port adjacent the proximal end of the cylinder in order to hydrate the bone graft material.

A surgical implant with recesses adapted to capture fixation medium that extravasates during implantation. The implant includes an elongated stem having a distal tip configured for insertion into an implant receiving area of a patient. A collar having recesses for capturing extravasating fixation medium is attached on the stem. The collar can be fixed to the stem by a separable collar-engagement feature or the collar can be fixed to the stem via structures on the stem.

A surgical implant with recesses adapted to capture fixation medium that extravazates during implantation. The implant includes an elongated stem having a distal tip configured for insertion into an implant receiving area of a patient. A collar designed to house recesses for capturing extravazating fixation medium is attached on the stem. The collar can be fixed to the stem by a separable collar-engagement feature or the collar can be fixed to the stem via structures on the stem.

A medical implant comprises a slurry of bone particles that are injected into a vertebral body under pressure. The liquid component of the slurry may be aspirated while the slurry is being injected so that the bone particles of the slurry pack into the central area of the vertebral body to provide structural support. The injected slurry may be agitated during the procedure to maximize the structural strength of the implant after the procedure.