Worldwide Distribution: US (nationwide) and countries of: Argentina, Australia, Brazil, Bolivia, Canada, Chile, China, Colombia, Ecuador, El Salvador, India, Japan, Malaysia, Mexico, Netherlands, New Zealand, Nicaragua, Panama, Seoul-Korea, Singapore, Taiwan, Thailand, and UAE.
Description du dispositif
CR PRECOAT FEM COMP SIZE BMR || CR PRECOAT FEM COMP SIZE C/R || CR PRECOAT FEM COMP SIZE D/R || CR PRECOAT FEM COMP SIZE E/R || CR PRECOAT FEM COMP SIZE F/R || CR PRECOAT FEM COMP SIZE G/L || CR PRECOAT FEM COMP SIZE H/L || CR PRECOAT FEM COMP SIZE H/R || CR POROUS FEM COMP SIZE E/L || CR POROUS FEM COMP SIZE H/R || This device is indicated for patients with severe knee pain and disability
“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 - US (nationwide) and Internationally to ARGENTINA AUSTRALIA AUSTRIA BARBADOS BELGIUM BERMUDA BOLIVIA BRAZIL CARIBBEAN CHILE CHINA COLOMBIA COST RICA DENMARK DOMINICAN REPUBLIC DORAL FL ECUADOR EL SALVADOR ENGLAND FRANCE GERMANY GUATEMALA HONDURAS HONG KONG INDIA ISRAEL ITALY JAMAICA JAPAN KOREA MALAYSIA MEXICO NEW ZEALAND NICARAGUA PANAMA PERU SINGAPORE SPAIN SWEDEN SWITZERLAND TAIWAN THAILAND VENEZUELA WEST INDIES Canary Islands Croatia Cyprus Czech Republic Canada
Description du dispositif
NexGen Knee CR Option Fem || NexGen Knee CR Porous Fem || NexGen Knee CR Precoat Fem || NexGen Knee LPS Porous Fem || NexGen Knee LPS Precoat Fem || prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer/metal/polymer || various sizes || This device is indicated for patients with severe knee pain and disability due to: Rheumatoid arthritis, osteoarthritis, traumatic arthritis, polyarthritis. Collagen disorders, and/or avascular necrosis of the femoral condyle. Post-traumatic loss of joint configuration, particularly when there is patellofemoral erosion, dysfunction or prior patellectomy. Moderate valgus, varus, or flexion deformities. The salvage of previously failed surgical attempts or for a knee in which satisfactory stability in flexion cannot be obtained at the time of surgery. " CR and LPS porous coated femoral and tibial baseplate components may be used cemented or uncemented (biological fixation). The CR Hydroxyapatite/tricalcium phosphate [HA/TCP] coated femoral or tibial baseplate components may only be used uncemented. All other femoral, tibial baseplate and all-polyethylene patella components are indicated for cemented use only."
Worldwide Distribution: US (nationwide) and countries of: Argentina, Australia, Brazil, Bolivia, Canada, Chile, China, Colombia, Ecuador, El Salvador, India, Japan, Malaysia, Mexico, Netherlands, New Zealand, Nicaragua, Panama, Seoul-Korea, Singapore, Taiwan, Thailand, and UAE.
Description du dispositif
CR OPTION FEM COMP SIZE C/L || CR OPTION FEM COMP SIZE C/R || CR OPTION FEM COMP SIZE D/L || CR OPTION FEM COMP SIZE D/R || CR OPTION FEM COMP SIZE E/L || CR OPTION FEM COMP SIZE E/R || CR OPTION FEM COMP SIZE F/L || CR OPTION FEM COMP SIZE F/R || CR OPTION FEM COMP SIZE G/L || CR OPTION FEM COMP SIZE G/R || This device is indicated for patients with severe knee pain and disability