Arthrosurfacer Inc

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Contact: Steven J. Tallarida - President
Web: http://www.arthrosurface.com
E-Mail:
Address: 28 Forge Parkway, Franklin, Massachusetts 02038, USA
Phone: +1-(508)-520-3003 | Fax: +1-(508)-528-4604 | Map/Directions >>

Profile: Arthrosurfacer Inc develops surgical equipments for the treatment of orthopedic joint disease. Arthrosurfacer launched a system to repair concave surfaces such as the tibial plateau, glenoid, the socket of the hip and other joint surfaces. Arthrosurfacer offers product for the treatment of articular cartilage defects in the knee, hip, shoulder & foot/ankle. The Arthrosurface HemiCAPr system is a surgical method for the treatment of localized cartilage lesions and defects in the major joints. The CAPr system aligns the surface of the implant to the contours of the patient's articular cartilage surface, thus filling the defect and restoring a smooth & continuous articular surface. The HemiCAPr implant is also used to address a full-cartilage defect in the shoulder associated with a rotator cuff injury. The HemiCAPr implants and instruments are designed to remove a minimal amount of bone stock, preserve functional structures and tissues and allows removal in the event of revision.

The company was founded in 2002.

FDA Registration Number: 3004154314

10 Products/Services (Click for related suppliers)

• Foot & Ankle Implant Systems

• Hip Products

• Humeral (hemi-shoulder) Metallic Uncemented Prosthesis (FDA Code: HSD / 888.3690)

A shoulder joint humeral (hemi-shoulder) metallic uncemented prosthesis is a device made of alloys, such as cobalt-chromium-molybdenum. It has an intramedullary stem and is intended to be implanted to replace the articular surface of the proximal end of the humerus and to be fixed without bone cement (888.3027). This device is not intended for biological fixation.

• Knee Joint Femorotibial Metal/Polymer Non-constrained Cemented Prosthesis (FDA Code: HSX / 888.3520)

A knee joint femorotibial metal/polymer non-constrained cemented prosthesis is a device intended to be implanted to replace part of a knee joint. The device limits minimally (less than normal anatomic constraints) translation in one or more planes. It has no linkage across-the-joint. This generic type of device includes prostheses that have a femoral condylar resurfacing component or components made of alloys, such as cobalt-chromium-molybdenum, and a tibial component or components made of ultra-high molecular weight polyethylene and are intended for use with bone cement (888.3027).

• Knee Products

• Orthopedic Manual Surgical Instrument (FDA Code: LXH / 888.4540)

An orthopedic manual surgical instrument is a nonpowered hand-held device intended for medical purposes to manipulate tissue, or for use with other devices in orthopedic surgery. This generic type of device includes the cerclage applier, awl, bender, drill brace, broach, burr, corkscrew, countersink, pin crimper, wire cutter, prosthesis driver, extractor, file, fork, needle holder, impactor, bending or contouring instrument, compression instrument, passer, socket positioner, probe, femoral neck punch, socket pusher, reamer, rongeur, scissors, screwdriver, bone skid, staple driver, bone screw starter, surgical stripper, tamp, bone tap, trephine, wire twister, and wrench.

• Patello-Femoral Replacement System

• Phalangeal Hemi- Toe Prosthesis (FDA Code: KWD / 888.3730)

A toe joint phalangeal (hemi-toe) polymer prosthesis is a device made of silicone elastomer intended to be implanted to replace the base of the proximal phalanx of the toe.

• Resurfacing Femoral Hip Prosthesis (FDA Code: KXA / 888.3400)

A hip joint femoral (hemi-hip) metallic resurfacing prosthesis is a device intended to be implanted to replace a portion of the hip joint. This generic type of device includes prostheses that have a femoral resurfacing component made of alloys, such as cobalt-chromium-molybdenum.

• Semi-Constrained Patellofemoral Knee Prosthesis (FDA Code: KRR / 888.3540)

A knee joint patellofemoral polymer/metal semi-constrained cemented prosthesis is a two-part device intended to be implanted to replace part of a knee joint in the treatment of primary patellofemoral arthritis or chondromalacia. The device limits translation and rotation in one or more planes via the geometry of its articulating surfaces. It has no linkage across-the-joint. This generic type of device includes a component made of alloys, such as cobalt-chromium-molybdenum or austenitic steel, for resurfacing the intercondylar groove (femoral sulcus) on the anterior aspect of the distal femur, and a patellar component made of ultra-high molecular weight polyethylene. This generic type of device is limited to those devices intended for use with bone cement (888.3027). The patellar component is designed to be implanted only with its femoral component.