Product 21 consists of all product under product code: JDI and same usage: || Item no: || 811400218 CPT 12/14 COCR REVISION S || 811400318 CPT 12/14 COCR REVISION S || 811400420 CPT 12/14 COCR REVISION S || 811400423 CPT 12/14 COCR REVISION S || 811400426 CPT 12/14 COCR REVISION S || 811400010 CPT 12/14 COCR SIZE 0 EXT || 811400000 CPT 12/14 COCR SIZE 0 STD || 811400110 CPT 12/14 COCR SIZE 1 EXT || 811400100 CPT 12/14 COCR SIZE 1 STD || 811400210 CPT 12/14 COCR SIZE 2 EXT || 811400200 CPT 12/14 COCR SIZE 2 STD || 811400230 CPT 12/14 COCR SIZE 2 XEX || 811400310 CPT 12/14 COCR SIZE 3 EXT || 811400300 CPT 12/14 COCR SIZE 3 STD || 811400330 CPT 12/14 COCR SIZE 3 XEX || 811400410 CPT 12/14 COCR SIZE 4 EXT || 811400400 CPT 12/14 COCR SIZE 4 STD || 811400430 CPT 12/14 COCR SIZE 4 XEX || 811400510 CPT 12/14 COCR SIZE 5 EXT || 811400500 CPT 12/14 COCR SIZE 5 STD || 811400530 CPT 12/14 COCR SIZE 5 XEX || Product Usage: || Single/multiple component metallic bone fixation appliances and accessories are devices intended to be implanted consisting of one or more metallic components and their metallic fasteners. The devices contain a plate, a nail/plate combination, or a blade/plate combination that are made of alloys, such as cobalt-chromium-molybdenum, stainless steel, and titanium, that are intended to be held in position with fasteners, such as screws and nails, or bolts, nuts, and washers. These devices are used for fixation of fractures of the proximal or distal end of long bones, such as intracapsular, intertrochanteric, intercervical, supracondylar, or condylar fractures of the femur; for fusion of a joint; or for surgical procedures that involve cutting a bone. The devices may be implanted or attached through the skin so that a pulling force (traction) may be applied to the skeletal system.
“The safety of patients has always been, and continues to be, Zimmer Biomet’s top priority and it is our honor to be a leader in this industry for the past 90 years,” Zimmer Biomet told ICIJ in a statement. “We adhere to strict regulatory standards, and work closely with the FDA and all applicable regulatory agencies in each of our regions as part of our commitment to operating a first-rate quality management system across our global manufacturing network. The company added that it is focused on staying at the forefront of innovation and doing right by the millions of patients who rely on the company’s products.
Worldwide Distribution --- USA including states of California, Minnesota, Ohio, Pennsylvania, and Tennessee, and countries of Denmark, Germany, Iran, Italy, Russia, Singapore, Spain, Switzerland, and United Kingdom.
Description du dispositif
Zimmer Silhouette Axial Torque Handle, Zimmer Spine, Inc., Minneapolis, MN; REF 7010-0151-01. || Reusable instrument that is used to apply the appropriate torque to the lock nut that is part of the Silhouette Spinal Fixation System.
Worldwide Distribution --- including USA, Belgium, Czech Republic, Finland, Germany, Greece, Italy, Poland, Romania, Spain and United Kingdom.
Description du dispositif
Zimmer Minimally Invasive Solutions Technology Offset Rasp Handle, Left, 30 degrees, Zimmer, Warsaw, IN; REF 00-7806-035-01. || The offset rasp handle is a surgical instrument used with various sizes of femoral rasps to prepare the femoral canal for a hip implant.
Nationwide, Canada, Denmark, Finland, Germany, Poland, Spain, Sweden and United Kingdom.
Description du dispositif
Zimmer NEXGEN Complete Knee Solution Cruciate Retaining (CR) Provisional - Articular surface, Size Blue, 14 MM Height, nonsterile, Zimmer, Warsaw, IN; REF 5971-50-14. || Used during total knee arthroplasty surgery to determine the required thickness of the tibial bearing surface to be implanted. Reusable, non-implantable.
Nationwide, Canada, Denmark, Finland, Germany, Poland, Spain, Sweden and United Kingdom.
Description du dispositif
Zimmer NEXGEN Complete Knee Solution Cruciate Retaining (CR) Provisional - Articular surface, Size Blue, 12 MM Height, nonsterile, Zimmer, Warsaw, IN; REF 5971-50-12. || Used during total knee arthroplasty surgery to determine the required thickness of the tibial bearing surface to be implanted. Reusable, non-implantable.
Nationwide Distribution --- including states of Arkansas, Florida, Michigan, North Carolina, New York and Wisconsin.
Description du dispositif
Zimmer Natural-Knee II System Modular Cemented Tibial Baseplate, Right, Size 3, For cemented use only, sterile, Zimmer, Warsaw, IN; REF 6420-01-230. || The modular cemented tibial baseplate is indicated for cemented use only in skeletally mature individuals with conditions of Noninflammatory Degenerative Joint Disease (NIDJD) or Inflammatory Joint Disease (IJD), correctable valgus-varus deformity and moderate flexion contracture, or failed previous surgery where pain, deformity or dysfunction persists. When the primary or N-K II Constrained Knee System components are used, the medial and collateral ligaments must be intact. || These are single use implantable devices sold sterile.