The Integra External Fixation System 5/8 ring is used for stability and structure. It is manufactured from aluminum. It is intended for the treatment of bone conditions including leg lengthening, osteotomies, arthrodesis, fracture fixation, and other bone conditions amenable to treatment by use of external fixation.

The Integra External Fixation System full ring is used for stability and structure. It is manufactured from aluminum. It is intended for the treatment of bone conditions including leg lengthening, osteotomies, arthrodesis, fracture fixation, and other bone conditions amenable to treatment by use of external fixation.

The Integra External Fixation System half ring is used for stability and structure. It is manufactured from aluminum. It is intended for the treatment of bone conditions including leg lengthening, osteotomies, arthrodesis, fracture fixation, and other bone conditions amenable to treatment by use of external fixation.

The Integra External Fixation System anterior half ring is used for stability and structure. It is manufactured from aluminum. It is intended for the treatment of bone conditions including leg lengthening, osteotomies, arthrodesis, fracture fixation, and other bone conditions amenable to treatment by use of external fixation.

The Integra External Fixation System footplate is used for stability and structure. It is manufactured from aluminum. It is intended for the treatment of bone conditions including leg lengthening, osteotomies, arthrodesis, fracture fixation, and other bone conditions amenable to treatment by use of external fixation.

The Integra External Fixation System 5/8 ring is used for stability and structure. It is manufactured from aluminum. It is intended for the treatment of bone conditions including leg lengthening, osteotomies, arthrodesis, fracture fixation, and other bone conditions amenable to treatment by use of external fixation.

The Integra External Fixation System full ring is used for stability and structure. It is manufactured from aluminum. It is intended for the treatment of bone conditions including leg lengthening, osteotomies, arthrodesis, fracture fixation, and other bone conditions amenable to treatment by use of external fixation.

The Integra External Fixation System half ring is used for stability and structure. It is manufactured from aluminum. It is intended for the treatment of bone conditions including leg lengthening, osteotomies, arthrodesis, fracture fixation, and other bone conditions amenable to treatment by use of external fixation.

The Integra External Fixation System anterior half ring is used for stability and structure. It is manufactured from aluminum. It is intended for the treatment of bone conditions including leg lengthening, osteotomies, arthrodesis, fracture fixation, and other bone conditions amenable to treatment by use of external fixation.

The Integra External Fixation System footplate is used for stability and structure. It is manufactured from aluminum. It is intended for the treatment of bone conditions including leg lengthening, osteotomies, arthrodesis, fracture fixation, and other bone conditions amenable to treatment by use of external fixation.

The Integra External Fixation System 5/8 ring is used for stability and structure. It is manufactured from aluminum. It is intended for the treatment of bone conditions including leg lengthening, osteotomies, arthrodesis, fracture fixation, and other bone conditions amenable to treatment by use of external fixation.

The Integra External Fixation System full ring is used for stability and structure. It is manufactured from aluminum. It is intended for the treatment of bone conditions including leg lengthening, osteotomies, arthrodesis, fracture fixation, and other bone conditions amenable to treatment by use of external fixation.

The Integra External Fixation System half ring is used for stability and structure. It is manufactured from aluminum. It is intended for the treatment of bone conditions including leg lengthening, osteotomies, arthrodesis, fracture fixation, and other bone conditions amenable to treatment by use of external fixation.

The Integra External Fixation System anterior half ring is used for stability and structure. It is manufactured from aluminum. It is intended for the treatment of bone conditions including leg lengthening, osteotomies, arthrodesis, fracture fixation, and other bone conditions amenable to treatment by use of external fixation.

The Integra External Fixation System 5/8 ring is used for stability and structure. It is manufactured from aluminum. It is intended for the treatment of bone conditions including leg lengthening, osteotomies, arthrodesis, fracture fixation, and other bone conditions amenable to treatment by use of external fixation.

The Integra External Fixation System full ring is used for stability and structure. It is manufactured from aluminum. It is intended for the treatment of bone conditions including leg lengthening, osteotomies, arthrodesis, fracture fixation, and other bone conditions amenable to treatment by use of external fixation.

The Integra External Fixation System half ring is used for stability and structure. It is manufactured from aluminum. It is intended for the treatment of bone conditions including leg lengthening, osteotomies, arthrodesis, fracture fixation, and other bone conditions amenable to treatment by use of external fixation.

The Integra External Fixation System 5/8 ring is used for stability and structure. It is manufactured from aluminum. It is intended for the treatment of bone conditions including leg lengthening, osteotomies, arthrodesis, fracture fixation, and other bone conditions amenable to treatment by use of external fixation.

The Integra External Fixation System half ring is used for stability and structure. It is manufactured from aluminum. It is intended for the treatment of bone conditions including leg lengthening, osteotomies, arthrodesis, fracture fixation, and other bone conditions amenable to treatment by use of external fixation.

A crossbar is manufactured from stainless steel and aluminum. It may be attached to the anterior ring for additional support.

A crossbar is manufactured from stainless steel and aluminum. It may be attached to the anterior ring for additional support.

The Integra External Fixation System two-post bridge is manufactured from stainless steel. It is intended for the treatment of bone conditions including leg lengthening, osteotomies, arthrodesis, fracture fixation, and other bone conditions amenable to treatment by use of external fixation.

A rockerbottom is attached to the bottom of the external device so that the patient may stand on it if needed. It is manufactured from aluminum and silicone rubber.

The Definitive Stem Reverse Shoulder Body Trial is used to evaluate the size and fit of the implant.

The Definitive Stem Reverse Shoulder Body Trial is used to evaluate the size and fit of the implant.

The Definitive Stem Reverse Shoulder Body Trial is used to evaluate the size and fit of the implant.

The Integra First Choice DRUJ System is intended for replacement of the distal radio-ulnar joint for rheumatoid, degenerative, or post traumatic arthritis. The set includes head and stem trials to evaluate the size and fit of the appropriate implant. Instruments are also included to assist with the trials.

The Titan Humeral Resurfacing Arthroplasty system is intended for resurfacing of the humeral head due to non-inflammatory or inflammatory arthritis, mild or moderate humeral head deformity and/or limited motion, post-traumatic arthritis, and patients with an intact or reparable rotator cuff. The set includes HRA trials to evaluate the size and fit of the appropriate implant, as well as sizers to determine the amount of bone resection needed for the implant. Instruments are also included to assist with the trials.

The Titan Modular Total Shoulder system is indicated for painful and/or disabled joints, fracture-dislocations, and other difficult clinical problems where shoulder arthrodesis or resection arthroplasty are not acceptable. The set includes cemented long stem trials and definitive stem primary body trials to evaluate the size and fit of the implant. Instruments are included to assist with the stem trials.

The Movement Great Toe System is used for hemi- and total-arthroplasty procedures. The hemi arthroplasty is intended for resurfacing of the 1st metatarsal head or the base of the proximal phalanx. The total arthroplasty is intended for resurfacing of the base of the 1st metatarso-phalangeal joint. This set includes metatarsal, proximal phalanx hemi, and proximal phalanx total trials to evaluate the size and fit of the appropriate implant. Instruments are also included to assist with the trials.

The Movement Great Toe System is used for hemi- and total-arthroplasty procedures. The hemi arthroplasty is intended for resurfacing of the 1st metatarsal head or the base of the proximal phalanx. The total arthroplasty is intended for resurfacing of the base of the 1st metatarso-phalangeal joint. This set includes metatarsal, proximal phalanx hemi, and proximal phalanx total trials to evaluate the size and fit of the appropriate implant. Instruments are also included to assist with the trials.

The Integra NuGrip system is intended to replace the proximal end of the first metacarpal in cases of rheumatoid arthritis, traumatic arthritis, osteo-arthritis or post fracture deformation of bone loss which present as either a painful, unstable thumb, or a thumb with limited range of motion. This set includes trials to evaluate the size and fit of the implant. Instruments are included for assistance.

Ascension® PIPThe PIP disposable pack for Stryker includes a blade, a side burr, a planer burr, and a guide pin.

The Ascension® PyroHemiSphereTM is intended to replace the proximal end of the first metacarpal in cases of rheumatoid arthritis, traumatic arthritis, osteoarthritis or post fracture deformation or bone loss which present as either a painful, unstable thumb, or a thumb with limited range of motion.

The Integra Lunate system is intended for replacement of the lunate bone in the proximal carpal row of the wrist. The set includes five trials to evaluate the size and fit of the implant. Five sizing templates are also included to assess coverage and establish proper sizing for the component.

The Ascension MCP is indicated for use as a total joint replacement of index, long, ring, and small finger metacarpophalangeal (MCP) joints that exhibit symptoms of pain, limited motion, or inadequate bony alignment secondary to articular destruction or degenerative disease related to rheumatoid arthritis, systemic lupus erythematosus, osteoarthritis, or post-traumatic arthritis where soft tissue reconstruction can provide adequate stabilization. The set includes proximal trials, distal trials, and silicone trials to evaluate the size and fit of the appropriate implant. Instruments are included to assist with the trials.

The Integra PyroCarbon PIP is indicated for use in arthroplasty of the proximal interphalangeal (PIP) joint when the patient has soft tissue and bone that can provide adequate stabilization and fixation under high-demand loading conditions after reconstruction, and when the patient needs a revision of a failed PIP prosthesis, or has pain, limited motion, or joint subluxation/dislocation secondary to damage or destruction of the articular cartilage. This set includes proximal and distal trials to evaluate proper size and fit of the implants. Instruments are included for assistance.

The Integra Silicone PIP is intended for replacement of the proximal interphalangeal (PIP) joint where disabled by rheumatoid, degenerative, or traumatic arthritis. This set includes silicone PIP trials to evaluate size and fit of the implants. Instruments are also included.

The Titan Modular Total Shoulder System humeral set 2.5 consists of body trials and humeral stem trials. A locking body screw is included for implantation. Instruments are provided to facilitate the placement of the trials and screw. The Titan Modular Total Shoulder system is indicated for painful and/or disabled joints, fracture-dislocations, and other difficult clinical problems where shoulder arthrodesis or resection arthroplasty are not acceptable.

The Humeral Stem Trial is used to evaluate the size and fit of the implant.

The Humeral Stem Trial is used to evaluate the size and fit of the implant.

The Humeral Stem Trial is used to evaluate the size and fit of the implant.

The Humeral Stem Trial is used to evaluate the size and fit of the implant.

The Humeral Stem Trial is used to evaluate the size and fit of the implant.

The Humeral Stem Trial is used to evaluate the size and fit of the implant.

The Titan Modular Total Shoulder System Humeral tray consists of body trials and humeral stem trials. A locking body screw is included for implantation. Instruments are provided to facilitate the placement of the trials and screw. The Titan Modular Total Shoulder system is indicated for painful and/or disabled joints, fracture-dislocations, and other difficult clinical problems where shoulder arthrodesis or resection arthroplasty are not acceptable.

The Integra External Fixation System set consists of wires, half-pins, nuts, and bolts. Instruments are also included to aid in assembly. The external fixation device is intended for use in the treatment of bone conditions including leg lengthening, osteotomies, arthrodesis, fracture fixation, and other bone conditions amenable to treatment by use of the external fixation modality.

The Integra External Fixation System set consists of struts, rods, and hex posts. These devices are used for support in the construct. Plates and a universal joint are also included. The external fixation device is intended for use in the treatment of bone conditions including leg lengthening, osteotomies, arthrodesis, fracture fixation, and other bone conditions amenable to treatment by use of the external fixation modality.

The Integra External Fixation System set consists of rings, footplates, anterior cross bars, and a rockerbottom. These devices are used for stability and structure. The external fixation device is intended for use in the treatment of bone conditions including leg lengthening, osteotomies, arthrodesis, fracture fixation, and other bone conditions amenable to treatment by use of the external fixation modality.

The Integra External Fixation System set consists of rings and footplates. These devices are used for stability and structure. The external fixation device is intended for use in the treatment of bone conditions including leg lengthening, osteotomies, arthrodesis, fracture fixation, and other bone conditions amenable to treatment by use of the external fixation modality.