Abstract: The invention relates to a disc-shaped augmentation for filling bone defects, in particular at the end of long bones, such as the tibia, comprising a proximal side (12), a distal side (II), an outer casing (15) on lateral sides and an inner wall for a through-opening (2), running from the proximal to the distal side, for a stabilising keel (8) of an endoprosthesis (9) arranged on the proximal side. The augmentation is generally C-shaped with two sections (31, 32) flanking the through-opening. According to the invention, a connection part (30) is formed in an articulated manner between the flanking sections (31, 32) and elastically cooperating with the flanking sections (31, 32).

Abstract: An augment device for a joint endoprosthesis, the device comprising: a sleeve having a top and a bottom, a distance between said top and said bottom defining an entire height of said sleeve, wherein the sleeve surrounds a channel extending through the sleeve from the top to the bottom of the sleeve wherein the channel is configured to receive a stem of the joint endoprosthesis; the sleeve comprising an inner face and an outer face, the inner face defining the channel, and a distance between the inner face and the outer face defining a thickness; the sleeve further comprising a porous material configured for ingrowth of bony material.

Abstract: The invention relates to an endoprosthesis shaft system for elongate bones, comprising an anchoring part and a shaft, which is formed from module elements that can be coupled by means of a plug-in connection, wherein a mutual rotation of the elements along the shaft is adjustable and is blocked by means of an anti-rotation mechanism. In order to adjust the rotation, a rotation piece is provided as a further module element, which has a self-contained rotation adjustment device and a clamping device as a mechanism for blocking the rotation. The rotation piece comprises two end faces for the plug-in connection and a sleeve. The invention provides, with the rotation piece, a particular module element for the shaft, which as a structural unit allows both an adjustment of the rotation and a blocking against undesired rotation in a self-contained unit.

Abstract: A coating for an implant component, in particular a component of a spinal implant. is provided. The coating is a ceramic titanium nitride coating comprising an at content of 5 to 30 At % of Ag in addition to an at % content of Ti and an at % content of N.

Abstract: The invention relates to a coating for an implant component, a method for producing an implant component having said coating, and a use of said coating on an implant component. The coating is intended for an implant component, in particular a spinal implant component, and is a TiNb coating which has, in addition to an atom % proportion of Ti and an atom % proportion of Nb, an atom % proportion of 5-30 atom % of Ag.

Abstract: An augment device for a joint endoprosthesis, the device comprising: a sleeve having a top and a bottom, a distance between said top and said bottom defining an entire height of said sleeve, wherein the sleeve surrounds a channel extending through the sleeve from the top to the bottom of the sleeve wherein the channel is configured to receive a stem of the joint endoprosthesis; the sleeve comprising an inner face and an outer face, the inner face defining the channel, and a distance between the inner face and the outer face defining a thickness; the sleeve further comprising a porous material configured for ingrowth of bony material.

Abstract: Devices and methods that include a structure configured to contact a portion of a mammal's bone; and a coating on at least a portion of the structure, wherein the coating comprises a titanium coating component, a silver coating component, and a nitrogen coating component.

Abstract: Implantable drug-eluting device comprising a microporous structure having regularly arranged pores in at least two different uniform sizes, and manufacturing method. The pores are configured for receiving a drug and are being connected by interconnections. Interconnections originating from pores of a first size have a first elution area and interconnections originating from pores of a second size have a second elution area. The interconnections convey the drug to a surface of the device for elution to surrounding tissue. The ratio between the first and the second elution areas is predefined and selectable. The differently sized elution areas provide for different outflow rates. This allows for simple but reliable dispensing of drugs at positively controlled and well determined rates. Particularly, this enables a single implantable device to dispense drugs over preselectable durations of time, like short-term or long-term.

Abstract: Disk-shaped augmentation for filling bone defects, in particular at the end of long bones, such as the tibia, including a first side, a second side, an outer sheath on lateral sides and an inner wall for a through-opening, running from the first to the second side, for a anchoring keel of an endoprosthesis arranged on the second side. The augment is generally C-shaped with two legs flanking the through-opening. According to the invention, a connecting piece between the legs is designed in an articulated manner and cooperates resiliently with the legs such that a frame is formed, and an outwardly directed restoring force is generated when the legs are compressed.

Abstract: A tibial component of a knee joint endoprosthesis includes a laterally extending tibial plate, a distally projecting anchoring stem with a shaft piece, and at least one laterally extending wing-like extension. In an implantation state, the tibial plate and the anchoring stem are connected to one another by means of detachable fastening elements. The tibial plate is removable from the anchoring stem for an explantation state. At least one spacer that can be removed proximally is provided on the tibial plate, the end face of which forms a stop for the extension and is designed to form a stop between the extension and the tibial plate to create space with a defined minimum width as a saw slot space.

Abstract: A coating for an implant component, in particular a component of a spinal implant, is provided. The coating is a ceramic titanium nitride coating comprising an at % content of 5 to 30 At % of Ag in addition to an at % content of Ti and an at % content of N.

Abstract: The invention relates to a coating for an implant component, a method for producing an implant component having said coating, and a use of said coating on an implant component. The coating is intended for an implant component, in particular a spinal implant component, and is a TiNb coating which has, in addition to an atom % proportion of Ti and an atom % proportion of Nb, an atom % proportion of 5-30 atom % of Ag.

Abstract: The disclosure includes an implant configured to contact a portion of a bone, the implant including a stem having a proximal section and a distal section and a porous portion extending a distance along the stem in a longitudinal direction of the stem.

Abstract: The present invention relates to an implant comprising an implant body having a first surface area configured for contact with soft connective tissue and a second surface area configured for contact with bone tissue, wherein the first surface area is covered with a coating comprising tantalum and the second surface area is formed by a material, which is different than the one forming the coating.

Abstract: The present invention provides a method for treating a polymer workpiece for use in a joint implant. It comprises the steps of placing the polymer workpiece in an explosion chamber, introducing a combustible gas mixture into the explosion chamber and igniting the combustible gas mixture. Igniting the gas mixture in the explosion chamber produces a temperature that lies above the melting point of a polymer of the polymer workpiece.

Abstract: 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.

Abstract: The present invention provides an active substance application insert for an implant, in particular a joint implant. The active substance application insert has a main body, an active substance chamber formed in the main body, an application side which forms a front face of the active substance chamber, wherein the application side has a plurality of application openings, and a securing means with which the main body can be detachably secured in the implant. In a state in which the main body is inserted into the implant, the application side faces outwards relative to the implant, such that the application openings connect the active substance chamber to the environment of the implant. Furthermore, within the scope of the present invention an implant with a recess for receiving an active substance application insert is provided.

Abstract: A pelvic implantation device that includes at least two outwardly directed, flat, fastening brackets arranged at an edge of a fastening ring, the fastening ring forming an opening; and a socket support body that includes a convex outer face configured to contact a pelvic bone; a distal edge that extends substantially orthogonally from a circumferential surface of the socket support body; and a tab, wherein the tab forms a portion of the circumferential surface of the socket support body, the tab including a proximal edge that extends substantially orthogonally from a surface of the tab, wherein the distal edge and the proximal edge are configured to contact an upper surface of the fastening ring.

Abstract: 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.

Abstract: The present invention provides an active substance application insert (10, 110) for an implant (30), in particular a joint implant. The active substance application insert has a main body (11), an active substance chamber (12) formed in the main body, an application side (13, 113) which forms a front face of the active substance chamber, wherein the application side has a plurality of application openings (14, 114), and a securing means (15) with which the main body can be detachably secured in the implant. In a state in which the main body is inserted into the implant, the application side faces outwards relative to the implant, such that the application openings connect the active substance chamber to the environment of the implant. Furthermore, within the scope of the present invention an implant (30) with a recess (31) for receiving an active substance application insert (10, 110) is provided.