A method for implantation of a locking member in a hip joint of a patient is disclosed. The method comprises; performing an operation in a hip joint surgically or arthroscopically, placing an artificial hollow caput femur surface mounted onto caput femur, placing a locking member for assisting in the fixation of the artificial caput femur surface with at least one extending portion adapted to clasp a portion of the caput and/or collum femur. The locking member comprises an element locking the artificial caput femur surface such that the caput femur remains clasped and restrained in said artificial caput femur surface.

An embodiment includes an expandable intervertebral body fusion device with two expansion wedges within a generally hollow main body. After implantation into the intervertebral disc space, the expansion wedges are simultaneously moved from the center of the device toward the ends, which flexes the arms of the cage and increases the size of the implant. This expansion stabilizes the device in the disc space and increases the disc height, thereby reducing foraminal compression of spinal nerves and creating a stable motion segment for eventual fusion. Other embodiments are described herein.

An expandable medical implant is provided with an implantable cage body. Methods for stabilizing and correcting the alignment of a spine with an expandable medical implant are provided. The proximal and distal ends of the cage body may each be provided with a plug for causing expansion of the ends of the implant and therefore the bone engaging surfaces of the implant. The proximal plug member may be configured to move longitudinally such that the proximal end of the cage body resiliently expands. The distal plug member may be configured to move longitudinally such that the distal end of the cage body resiliently expands. The proximal and distal plug members are moved longitudinally independently from one another to allow for independent expansion and contraction of each of the proximal and distal ends of the cage body itself.

An augment device includes a hollow sleeve surrounding a channel extending through the hollow sleeve from a top to a bottom of the hollow sleeve, the hollow sleeve comprising a wall having an inner face and an outer face. The hollow sleeve includes at least one bending joint, the bending joint being configured for compressing the channel. Thereby the hollow sleeve may be compressed under an external force, leading to a decreased circumference and width of the hollow sleeve. This leads to a gap between the perimeter of the augment device and surrounding bone material, breaking any connections. By virtue of this, a much facilitated removal of the augment device can be achieved. Further, an extraction tool includes grippers for engaging and compressing the augment device, and further instruments, particularly a jig, for achieving an effective removal.

A system and methods for a safe and efficient distributing of bone graft material into an intervertebral disc space are provided. Systems are provided for receiving, removing, and replacing of preloaded load cartridges in a rapid and repeating manner. The systems can also be designed for rapidly delivering the biologics from a single load cartridge and, to even further facilitate a rapid and repeating delivery of biologics, the load cartridge and cartridge tamp can be adapted so that the cartridge tamp can capture and remove the load cartridge after delivery of fusion promoting material in the load cartridge.

An interbody device may include a main body and an arm movably connected thereto. The device may have a first end, a second end opposite the first end in a direction of a longitudinal axis of the device, a first side, a second side opposite the first side in a direction of a first transverse axis of the device, a third side, and a fourth side opposite the third side in a direction of a second transverse axis of the device. An overall distance between the first side and the second side may increase along at least a majority of a length of the device in a direction from the first end toward the second end, and an overall distance between the third side and the fourth side may increase along at least a majority of the length in a direction from the second end toward the first end.

The present invention relates generally to a prosthetic spinal disc for replacing a damaged disc between two vertebrae of a spine. The present invention also relates to a method for implanting a prosthetic spinal disc via anterior or anterior lateral implantation. Other surgical approaches for implanting the prosthetic disc may also be used.

The disclosure relates to a scaffold for tissue regeneration and methods for fabricating the scaffold. The scaffold includes a three-dimensional structure composed by alternating layers of various materials including a first medium, a second medium and a third medium. The first medium includes bone particles each having a size of 1 nm to 100 mm with or without organic components. The second medium is a natural or synthetic biocompatible and/or biodegradable polymer. The third medium is a material dissolved in a solvent different than the solvent of the polymer and includes solid particulates alone or in polymeric structures that dissolve when immersed in liquid or gaseous solvent environments or based on temperature differentials. The various materials are arranged according to the shape and the size of a bone gap being generated. The three-dimensional structure has a tunable porosity with interconnected channels and pores along with adjustable dimensions.

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.

An expandable medical implant is provided with an implantable cage body. Methods for stabilizing and correcting the alignment of a spine with an expandable medical implant are provided. The proximal and distal ends of the cage body may each be provided with a plug for causing expansion of the ends of the implant and therefore the bone engaging surfaces of the implant. The proximal plug member may be configured to move longitudinally such that the proximal end of the cage body resiliently expands. The distal plug member may be configured to move longitudinally such that the distal end of the cage body resiliently expands. The proximal and distal plug members are moved longitudinally independently from one another to allow for independent expansion and contraction of each of the proximal and distal ends of the cage body itself.