The invention relates to a shaft for a femoral neck prosthesis, which comprises an anchoring area (27, 29) which is arranged inside the femur in order to anchor the prosthesis into bone, a head area which is axially adjacent to the anchoring area (27, 29) on the proximal side, said head area comprising a device (13) which is connected to the prosthesis head (15), in addition to a distal end which is arranged opposite the head area in the axial direction of the anchoring area (27, 29). The invention is characterised in that the maximum cross-sectional dimension of the head area is at the most equal and, in particular, smaller than the maximum diameter of the anchoring area (27, 29), in such a manner that the maximum cross-sectional dimension of the shaft (11) is in the anchoring area (27, 29).

An injection device for use in sacroiliac joint stabilization comprises an elongated conduit having a first end and a second end, where the first end includes a first opening and the second end includes a second opening; a carrier member couplable with the conduit and configured to accommodate a guidewire; a tool configured to be at least partially disposed in a bore of the conduit via the second opening, where the tool is configured to urge a hardening material in the bore toward the first end of the conduit; where the first opening of the conduit is configured to be angularly disposed relative to the second opening of the conduit such that the first end directs hardening material in a non-parallel direction relative to a longitudinal axis of the conduit.

A balloon, a medical device, and a medical procedure for discoplasty are disclosed. The balloon has a compressed, collapsed or folded balloon body containing a first chamber for, in use, receiving injected bone cement. With the bone cement filled and cured therein, the balloon acts as a support in tissue of an intervertebral disc while preventing the bone cement from leakage and dispersion. The deployed balloon body defines a second chamber running therethrough. The second chamber is configured to receive a material or cells that activate osteogenesis and/or osteo-induction, so that the material or cells injected into the second chamber through a second sprue form osteocytes or induce human spontaneous local cellular differentiation to in turn form osteocytes in the cavity of the intervertebral disc and connect vertebrae above and below the intervertebral disc, thereby securely anchoring the balloon within the intervertebral space.

A device is disclosed that includes a bone stent positioned within a bony access channel formed within a vertebra. The bony access channel may extends from an outer end of the vertebra through an endplate. The device includes an end cap attached to a proximal end portion of the bone stent and is configured to, post-operatively, open to allow a reintroduction of a material to a spinal intradiscal space or intervertebral disc and to seal access to the spinal intradiscal space or the intervertebral disc after the reintroduction of the material.

The invention relates to an assembly (1) for positioning and positionally immobilizing an inflatable balloon (3) within a vertebral body, comprising an access piece (2) providing access to the vertebral body, which has a cannula and is of elongate shape, and an inflatable balloon (3) mounted at the end of a catheter (4) able to be connected to a fluid-delivery unit, the assembly comprising balloon (3) and catheter being designed to pass slidingly through the access piece (2), characterized in that the access piece (2) comprises means of anchorage in the vertebral body, the assembly further comprising means for positionally immobilizing the catheter provided with the balloon (3) on the access piece (2).

The present invention is a process of making a patient-specific implant for a patient. The current process is adaptable to manufacture spinal and other implants for insertion into the patient.

A device is disclosed that includes a bone stent positioned within a bony access channel formed within a vertebra. The bony access channel may extends from an outer end of the vertebra through an endplate. The device includes an end cap attached to a proximal end portion of the bone stent and is configured to, post-operatively, open to allow a reintroduction of a material to a spinal intradiscal space or intervertebral disc and to seal access to the spinal intradiscal space or the intervertebral disc after the reintroduction of the material.

A balloon, a medical device, and a medical procedure for discoplasty are disclosed. The balloon has a compressed, collapsed or folded balloon body containing a first chamber for, in use, receiving injected bone cement. With the bone cement filled and cured therein, the balloon acts as a support in tissue of an intervertebral disc while preventing the bone cement from leakage and dispersion. The deployed balloon body defines a second chamber running therethrough. The second chamber is configured to receive a material or cells that activate osteogenesis and/or osteo-induction, so that the material or cells injected into the second chamber through a second sprue form osteocytes or induce human spontaneous local cellular differentiation to in turn form osteocytes in the cavity of the intervertebral disc and connect vertebrae above and below the intervertebral disc, thereby securely anchoring the balloon within the intervertebral space.

Surgical systems, methods and surgical planning programs to facilitate preparation of an anatomical cavity to receive a cup implant. The system includes a control system, a localizer and a robotic manipulator configured to move an energy applicator that is adapted to remove tissue. The control system obtains or generates a surgical plan that defines characteristics of cement holes to be formed within a wall of the anatomical cavity for receiving bone cement. The control system registers the surgical plan to the anatomical cavity with the localizer and controls the robotic manipulator to utilize the energy applicator to form the cement holes within the wall of the anatomical cavity according to the surgical plan.