The Capture Digital screw is a cannulated, threaded bone screw made from titanium and is used for bone fixation of the hand and foot, following trauma or osteotomy.

The Capture Digital screw is a cannulated, threaded bone screw made from titanium and is used for bone fixation of the hand and foot, following trauma or osteotomy.

The Capture Digital screw is a cannulated, threaded bone screw made from titanium and is used for bone fixation of the hand and foot, following trauma or osteotomy.

The Capture Digital screw is a cannulated, threaded bone screw made from titanium and is used for bone fixation of the hand and foot, following trauma or osteotomy.

The Capture Digital screw is a cannulated, threaded bone screw made from titanium and is used for bone fixation of the hand and foot, following trauma or osteotomy.

The Capture Digital screw is a cannulated, threaded bone screw made from titanium and is used for bone fixation of the hand and foot, following trauma or osteotomy.

The Capture Digital screw is a cannulated, threaded bone screw made from titanium and is used for bone fixation of the hand and foot, following trauma or osteotomy.

The Capture Digital screw is a cannulated, threaded bone screw made from titanium and is used for bone fixation of the hand and foot, following trauma or osteotomy.

The Capture Digital screw is a cannulated, threaded bone screw made from titanium and is used for bone fixation of the hand and foot, following trauma or osteotomy.

The Capture Digital screw is a cannulated, threaded bone screw made from titanium and is used for bone fixation of the hand and foot, following trauma or osteotomy.

The Capture Digital screw is a cannulated, threaded bone screw made from titanium and is used for bone fixation of the hand and foot, following trauma or osteotomy.

The Capture Digital screw is a cannulated, threaded bone screw made from titanium and is used for bone fixation of the hand and foot, following trauma or osteotomy.

The Capture Digital screw is a cannulated, threaded bone screw made from titanium and is used for bone fixation of the hand and foot, following trauma or osteotomy.

The Capture Digital screw is a cannulated, threaded bone screw made from titanium and is used for bone fixation of the hand and foot, following trauma or osteotomy.

The Capture Digital screw is a cannulated, threaded bone screw made from titanium and is used for bone fixation of the hand and foot, following trauma or osteotomy.

The Capture Digital screw is a cannulated, threaded bone screw made from titanium and is used for bone fixation of the hand and foot, following trauma or osteotomy.

The Capture Digital screw is a cannulated, threaded bone screw made from titanium and is used for bone fixation of the hand and foot, following trauma or osteotomy.

The Capture Digital screw is a cannulated, threaded bone screw made from titanium and is used for bone fixation of the hand and foot, following trauma or osteotomy.

The Capture Digital screw is a cannulated, threaded bone screw made from titanium and is used for bone fixation of the hand and foot, following trauma or osteotomy.

The Capture Digital screw is a cannulated, threaded bone screw made from titanium and is used for bone fixation of the hand and foot, following trauma or osteotomy.

The Integra® BioMotion® Cannulated Hemi implant is used with the Integra® BioMotion® Cannulated Hemi System as a partial joint replacement for the first metatarsophalangeal joint (MPJ). The Cannulated Implants are made from Titanium Alloy (ASTM F-136).

The Integra® BioMotion® Cannulated Hemi implant is used with the Integra® BioMotion® Cannulated Hemi System as a partial joint replacement for the first metatarsophalangeal joint (MPJ). The Cannulated Implants are made from Titanium Alloy (ASTM F-136).

The Integra® BioMotion® Cannulated Hemi implant is used with the Integra® BioMotion® Cannulated Hemi System as a partial joint replacement for the first metatarsophalangeal joint (MPJ). The Cannulated Implants are made from Titanium Alloy (ASTM F-136).

The Integra® BioMotion® Cannulated Hemi implant is used with the Integra® BioMotion® Cannulated Hemi System as a partial joint replacement for the first metatarsophalangeal joint (MPJ). The Cannulated Implants are made from Titanium Alloy (ASTM F-136).

The Integra® BioMotion® Cannulated Hemi implant is used with the Integra® BioMotion® Cannulated Hemi System as a partial joint replacement for the first metatarsophalangeal joint (MPJ). The Cannulated Implants are made from Titanium Alloy (ASTM F-136).

Humeral Resurfacing Arthroplasty

Humeral Resurfacing Arthroplasty

Humeral Resurfacing Arthroplasty

Humeral Resurfacing Arthroplasty

Humeral Resurfacing Arthroplasty

Humeral Resurfacing Arthroplasty

The Ascension® PyroCarbon Lunate is an anatomically designed lunate replacement with essentially the same shape as the native lunate bone. The Lunate implant acts as an articulating spacer to maintain the relationship of adjacent carpal bones after excision and to maintain mobility of the wrist. The articular concavity that captures the capitate is more exaggerated to enhance stability. The Lunate implant has two suture holes which allow fixation of the implant to the adjacent scaphoid and triquetrium bones to provide temporary postoperative stability while a capsuloligamentous system forms around the implant. The Ascension® Pyrocarbon Lunate is constructed of a high strength On-X® PyroCarbon layer deposited on a graphite substrate. The graphite is impregnated with tungsten making the Lunate implant radiopaque. The Ascension® PyroCarbon Lunate is intended for replacement of the lunate bone in the proximal carpal row of the wrist in the presence of Avascular necrosis (Kienboch’s disease), localized osteoarthritic, or changes in Long-Standing dislocations.

The Ascension® PyroCarbon Lunate is an anatomically designed lunate replacement with essentially the same shape as the native lunate bone. The Lunate implant acts as an articulating spacer to maintain the relationship of adjacent carpal bones after excision and to maintain mobility of the wrist. The articular concavity that captures the capitate is more exaggerated to enhance stability. The Lunate implant has two suture holes which allow fixation of the implant to the adjacent scaphoid and triquetrium bones to provide temporary postoperative stability while a capsuloligamentous system forms around the implant. The Ascension® Pyrocarbon Lunate is constructed of a high strength On-X® PyroCarbon layer deposited on a graphite substrate. The graphite is impregnated with tungsten making the Lunate implant radiopaque. The Ascension® PyroCarbon Lunate is intended for replacement of the lunate bone in the proximal carpal row of the wrist in the presence of Avascular necrosis (Kienboch’s disease), localized osteoarthritic, or changes in Long-Standing dislocations.

The Ascension® PyroCarbon Lunate is an anatomically designed lunate replacement with essentially the same shape as the native lunate bone. The Lunate implant acts as an articulating spacer to maintain the relationship of adjacent carpal bones after excision and to maintain mobility of the wrist. The articular concavity that captures the capitate is more exaggerated to enhance stability. The Lunate implant has two suture holes which allow fixation of the implant to the adjacent scaphoid and triquetrium bones to provide temporary postoperative stability while a capsuloligamentous system forms around the implant. The Ascension® Pyrocarbon Lunate is constructed of a high strength On-X® PyroCarbon layer deposited on a graphite substrate. The graphite is impregnated with tungsten making the Lunate implant radiopaque. The Ascension® PyroCarbon Lunate is intended for replacement of the lunate bone in the proximal carpal row of the wrist in the presence of Avascular necrosis (Kienboch’s disease), localized osteoarthritic, or changes in Long-Standing dislocations.

The Ascension® PyroCarbon Lunate is an anatomically designed lunate replacement with essentially the same shape as the native lunate bone. The Lunate implant acts as an articulating spacer to maintain the relationship of adjacent carpal bones after excision and to maintain mobility of the wrist. The articular concavity that captures the capitate is more exaggerated to enhance stability. The Lunate implant has two suture holes which allow fixation of the implant to the adjacent scaphoid and triquetrium bones to provide temporary postoperative stability while a capsuloligamentous system forms around the implant. The Ascension® Pyrocarbon Lunate is constructed of a high strength On-X® PyroCarbon layer deposited on a graphite substrate. The graphite is impregnated with tungsten making the Lunate implant radiopaque. The Ascension® PyroCarbon Lunate is intended for replacement of the lunate bone in the proximal carpal row of the wrist in the presence of Avascular necrosis (Kienboch’s disease), localized osteoarthritic, or changes in Long-Standing dislocations.

The Ascension® PyroCarbon Lunate is an anatomically designed lunate replacement with essentially the same shape as the native lunate bone. The Lunate implant acts as an articulating spacer to maintain the relationship of adjacent carpal bones after excision and to maintain mobility of the wrist. The articular concavity that captures the capitate is more exaggerated to enhance stability. The Lunate implant has two suture holes which allow fixation of the implant to the adjacent scaphoid and triquetrium bones to provide temporary postoperative stability while a capsuloligamentous system forms around the implant. The Ascension® Pyrocarbon Lunate is constructed of a high strength On-X® PyroCarbon layer deposited on a graphite substrate. The graphite is impregnated with tungsten making the Lunate implant radiopaque. The Ascension® PyroCarbon Lunate is intended for replacement of the lunate bone in the proximal carpal row of the wrist in the presence of Avascular necrosis (Kienboch’s disease), localized osteoarthritic, or changes in Long-Standing dislocations.

The Integra Movement Great Toe System metatarsal component is designed for resurfacing the 1st metatarsal head. The component is an anatomically designed, monolithic device.The device is made from cobalt chromium alloy with a commercially pure titanium plasma spray. The metatarsal is intended as hemi-arthroplasty at the surface and is a press-fit.

The Integra Movement Great Toe System phalangeal component is designed for resurfacing the base of the proximal phalanx. The component is an anatomically designed, monolithic device. The device is made from cobalt chromium alloy with a commerically pure titanium plasma spray. The phalangeal component is intended as hemi-arthroplasty at the surface and is press-fit.

The Integra Movement Great Toe System metatarsal component is designed for resurfacing the 1st metatarsal head. The component is an anatomically designed, monolithic device.The device is made from cobalt chromium alloy with a commercially pure titanium plasma spray. The metatarsal is intended as hemi-arthroplasty at the surface and is a press-fit.

The Integra Movement Great Toe System phalangeal component is designed for resurfacing the base of the proximal phalanx. The component is an anatomically designed, monolithic device. The device is made from cobalt chromium alloy with a commerically pure titanium plasma spray. The phalangeal component is intended as hemi-arthroplasty at the surface and is press-fit.

The Integra Movement Great Toe System metatarsal component is designed for resurfacing the 1st metatarsal head. The component is an anatomically designed, monolithic device.The device is made from cobalt chromium alloy with a commercially pure titanium plasma spray. The metatarsal is intended as hemi-arthroplasty at the surface and is a press-fit.

The Integra Movement Great Toe System phalangeal component is designed for resurfacing the base of the proximal phalanx. The component is an anatomically designed, monolithic device. The device is made from cobalt chromium alloy with a commerically pure titanium plasma spray. The phalangeal component is intended as hemi-arthroplasty at the surface and is press-fit.

The Integra Movement Great Toe System metatarsal component is designed for resurfacing the 1st metatarsal head. The component is an anatomically designed, monolithic device.The device is made from cobalt chromium alloy with a commercially pure titanium plasma spray. The metatarsal is intended as hemi-arthroplasty at the surface and is a press-fit.

The Integra Movement Great Toe System phalangeal component is designed for resurfacing the base of the proximal phalanx. The component is an anatomically designed, monolithic device. The device is made from cobalt chromium alloy with a commerically pure titanium plasma spray. The phalangeal component is intended as hemi-arthroplasty at the surface and is press-fit.

The Ascension silicone PIP is an anatomically designed, single use, one piece, flexible hinge prosthesis designed to be implanted without bone cement across the proximal interphalangeal (PIP) joint. It is made from medical grade silicone elastomer. The proximal and distal stems of the prosthesis are pre-flexed to match the approximate natural flexion position of the joint when the hand is relaxed. the PIP provides 90 degrees of flexion from full extension. The Ascension PIP finger joint prostheses is intended for cementless replacement of the proximal interphalangeal (PIP) joint where disabled by rheumatoid, degenerative, or traumatic arthritis.

The Ascension silicone PIP is an anatomically designed, single use, one piece, flexible hinge prosthesis designed to be implanted without bone cement across the proximal interphalangeal (PIP) joint. It is made from medical grade silicone elastomer. The proximal and distal stems of the prosthesis are pre-flexed to match the approximate natural flexion position of the joint when the hand is relaxed. the PIP provides 90 degrees of flexion from full extension. The Ascension PIP finger joint prostheses is intended for cementless replacement of the proximal interphalangeal (PIP) joint where disabled by rheumatoid, degenerative, or traumatic arthritis.

The Ascension silicone PIP is an anatomically designed, single use, one piece, flexible hinge prosthesis designed to be implanted without bone cement across the proximal interphalangeal (PIP) joint. It is made from medical grade silicone elastomer. The proximal and distal stems of the prosthesis are pre-flexed to match the approximate natural flexion position of the joint when the hand is relaxed. the PIP provides 90 degrees of flexion from full extension. The Ascension PIP finger joint prostheses is intended for cementless replacement of the proximal interphalangeal (PIP) joint where disabled by rheumatoid, degenerative, or traumatic arthritis.

The Ascension silicone PIP is an anatomically designed, single use, one piece, flexible hinge prosthesis designed to be implanted without bone cement across the proximal interphalangeal (PIP) joint. It is made from medical grade silicone elastomer. The proximal and distal stems of the prosthesis are pre-flexed to match the approximate natural flexion position of the joint when the hand is relaxed. the PIP provides 90 degrees of flexion from full extension. The Ascension PIP finger joint prostheses is intended for cementless replacement of the proximal interphalangeal (PIP) joint where disabled by rheumatoid, degenerative, or traumatic arthritis.

The Ascension silicone PIP is an anatomically designed, single use, one piece, flexible hinge prosthesis designed to be implanted without bone cement across the proximal interphalangeal (PIP) joint. It is made from medical grade silicone elastomer. The proximal and distal stems of the prosthesis are pre-flexed to match the approximate natural flexion position of the joint when the hand is relaxed. the PIP provides 90 degrees of flexion from full extension. The Ascension PIP finger joint prostheses is intended for cementless replacement of the proximal interphalangeal (PIP) joint where disabled by rheumatoid, degenerative, or traumatic arthritis.

The Ascension silicone PIP is an anatomically designed, single use, one piece, flexible hinge prosthesis designed to be implanted without bone cement across the proximal interphalangeal (PIP) joint. It is made from medical grade silicone elastomer. The proximal and distal stems of the prosthesis are pre-flexed to match the approximate natural flexion position of the joint when the hand is relaxed. the PIP provides 90 degrees of flexion from full extension. The Ascension PIP finger joint prostheses is intended for cementless replacement of the proximal interphalangeal (PIP) joint where disabled by rheumatoid, degenerative, or traumatic arthritis.