Transfemoral Percutaneous Prosthetic
FDA product code PJY · Class 3 · 16 devices · 144 reports · 0 devices named in recalls
- OPRA Implant System 1288Integrum AB · Transfemoral Percutaneous Prosthetic109 reports
- OPRA Implant System 1820Integrum AB · Transfemoral Percutaneous Prosthetic8 reports
- OPRA Implant System 1800Integrum AB · Transfemoral Percutaneous Prosthetic4 reports
- OPRA Implant System 1804Integrum AB · Transfemoral Percutaneous Prosthetic4 reports
- OPRA Implant System 1808Integrum AB · Transfemoral Percutaneous Prosthetic3 reports
- OPRA Implant System 1803Integrum AB · Transfemoral Percutaneous Prosthetic2 reports
- OPRA Implant System 1810Integrum AB · Transfemoral Percutaneous Prosthetic2 reports
- OPRA Implant System 1811Integrum AB · Transfemoral Percutaneous Prosthetic2 reports
- OPRA Implant System IBC0010Integrum AB · Transfemoral Percutaneous Prosthetic2 reports
- OPRA Implant System IBC0012Integrum AB · Transfemoral Percutaneous Prosthetic2 reports
- OPRA Implant System 1342Integrum AB · Transfemoral Percutaneous Prosthetic1 report
- OPRA Implant System 1348Integrum AB · Transfemoral Percutaneous Prosthetic1 report
- OPRA Implant System 1353Integrum AB · Transfemoral Percutaneous Prosthetic1 report
- OPRA Implant System 1805Integrum AB · Transfemoral Percutaneous Prosthetic1 report
- OPRA Implant System 1807Integrum AB · Transfemoral Percutaneous Prosthetic1 report
- OPRA Implant System 1959Integrum AB · Transfemoral Percutaneous Prosthetic1 report