A surgical pelvic drill for operating hip osteoarthritis adapted to create a hole in the pelvic bone of a human patient is provided. The pelvic drill is adapted to create a through-going hole placed in the acetabulum area from the abdominal side of the pelvic bone of the human patient. The pelvic drill comprises: a driving member, a bone contacting organ in connection with said driving member, an operating device adapted to operate said driving member. The bone contacting organ is adapted to create a hole in the acetabulum area starting from the abdominal side of the pelvic bone through repetitive or continuous movement. A surgical and a laparoscopic/arthroscopic method of using said pelvic drill is further provided.

An implant stabilizes two adjacent bones of a joint, while enabling a natural kinematic relative movement of the bones. Support components are connected to each bone of the joint, and a flexible core is interposed between them. The core and at least one of the support components are provided with a smooth sliding surface upon which the core and support component may slide relative to each other, enabling a corresponding movement of the bones. The surfaces may have a mating curvature, to mimic a natural movement of the joint. The core is resilient, and may bend or compress, enabling the bones to move towards each other, and or to bend relative to each other.

The disclosure provides a cartilage substitute, which includes at least one cartilage unit, the cartilage unit including: a base, including a subcutaneous layer portion forming contact friction with a corresponding skeleton, a deep layer area portion contacting with a target skeleton and an intermediate layer portion provided between the subcutaneous layer portion and the deep layer area portion. A fluid storage cavity is disposed in the subcutaneous layer portion. A first communicating passage is disposed in the subcutaneous layer portion. A second communicating passage is disposed in the intermediate layer portion, a third communicating passage is disposed in the deep layer area portion. The fluid storage cavity, the second communicating passage and the third communicating passage are disposed to gradually increase hardness of the subcutaneous layer portion, the intermediate layer portion and the deep layer area portion.

An intervertebral device comprises a plurality of struts that are rotatably associated with each adjacent strut to form a modifiable inner volume V for bone graft containment.

An orthopedic prosthesis includes a proximal member which internally accommodates the major motion of a patient, e.g., during walking, thereby reducing wear against a cup or liner. A distal member may be utilized which rotates within the distal member about an axis aligned with the major motion of the patient. The orthopedic prosthesis may also include a head and neck, the neck being rotatably mounted within the head, the head being rotatably mounted within the acetabulum region of a patient.

A mold adapted to be introduced into a joint of a human patient for resurfacing at least one carrying contacting surface of said joint is provided. The mold is adapted to receive material for resurfacing at least one carrying contacting surface of said joint. The mold is further adapted to be resorbed by the human body or melt after having served its purpose. Further, a method of treating hip joint osteoarthritis in a human patient by providing an artificial hip joint surface using a mold is provided. The method comprises the steps of: said mold being placed inside of said hip joint, said mold being injected with a fluid adapted to harden, said fluid hardening inside of said hip joint, said mold being resorbed by the human body, and said hardened fluid serving as artificial hip joint surface.

A prosthesis for a synovial joint arthroplasty within a human body is provided. The prosthesis includes a first prosthetic component, the first prosthetic component including a first surface and the first prosthetic component is formed of a plastic compound, the plastic compound includes a polymer, a plurality of long glass fibers, the long glass fibers being randomly dispersed throughout the polymer to improve surface fatigue life and inhibit surface crack propagation to the prosthesis and improve wear resistance of the prosthesis, a number of the plurality of long glass fibers configured to protrude outward from the first surface of the first prosthetic component, a plurality of beads, the beads being randomly dispersed throughout the polymer to improve surface fatigue life and inhibit surface crack propagation to the prosthesis and improve wear resistance of the prosthesis, a number of the plurality of beads configured to protrude outward from the first surface of the first prosthetic component, a second prosthetic component, the second prosthetic component including a second surface, the second surface of the second prosthetic component configured to engage said first surface of said first prosthetic component and slide relative to the first surface of the first prosthetic component while contacting the plurality of long glass fibers protruding outward from the first surface of the first prosthetic component and the plurality of beads protruding outward from the first surface of the first prosthetic component.

An implant stabilizes two adjacent bones of a joint, while enabling a natural kinematic relative movement of the bones. Support components are connected to each bone of the joint, and a flexible core is interposed between them. The core and at least one of the support components are provided with a smooth sliding surface upon which the core and support component may slide relative to each other, enabling a corresponding movement of the bones. The surfaces may have a mating curvature, to mimic a natural movement of the joint. The core is resilient, and may bend or compress, enabling the bones to move towards each other, and or to bend relative to each other.

An prosthetic implant replaces hyaline cartilage in a synovial joint with a flexible polymer sliding surface, preferably of hydrogel, on a segmented support with an array of adjacent segments to which the hydrogel is molded. Adjacent segments are laterally and angularly displaceable permitting the implant to conform to rounded or irregular surfaces or to be rolled or folded for arthroscopic placement. Tension cables threaded through segments along a circuit can cinch segments together for stiffening the supporting layer and/or the cable can pull the implant against a bone surface. Adjacent segments can have inter-engaged structures. In some embodiments the segments are carried on a flexible foil or fibrous sheet.

A medical device for implantation in a knee joint of a human patient is provided. The medical device comprises: an inner surface and an outer surface. The inner surface comprises: a first point, a second point, a third point, a fourth point, a fifth point, and a sixth point, all points located on different places along a length axis of said inner surface. A first straight line, reaching from the first point to the second point is parallel to a second straight line reaching from the third point to the fourth point, which in turn is parallel to a third straight line reaching from the fifth point to the sixth point. The first and third straight lines are of equal length and the second straight line is longer than the first, furthermore the third straight line is positioned between the first and third straight lines. Wherein the medical device comprises a first articulating surface adapted replaced the surface of the contacting surface of the medial condyle, a second articulating surface adapted to replace the contacting surface of the lateral condyle and a third articulating surface adapted to replace the contacting surface of the patella.