In Situ Polymerizing Peripheral Nerve Repair Device
FDA product code SFD · Class 2 · 8 devices · 2 reports · 8 devices named in recalls
- COAPTIUM® Connect NCOCO3010Tissium · In Situ Polymerizing Peripheral Nerve Repair Device1 recall1 report
- COAPTIUM® Connect NCOCO6010Tissium · In Situ Polymerizing Peripheral Nerve Repair Device1 recall1 report
- COAPTIUM® Connect NCOCO1510Tissium · In Situ Polymerizing Peripheral Nerve Repair Device1 recall0 reports
- COAPTIUM® Connect NCOCO1575Tissium · In Situ Polymerizing Peripheral Nerve Repair Device1 recall0 reports
- COAPTIUM® Connect NCOCO2010Tissium · In Situ Polymerizing Peripheral Nerve Repair Device1 recall0 reports
- COAPTIUM® Connect NCOCO2075Tissium · In Situ Polymerizing Peripheral Nerve Repair Device1 recall0 reports
- COAPTIUM® Connect NCOCO4010Tissium · In Situ Polymerizing Peripheral Nerve Repair Device1 recall0 reports
- COAPTIUM® Connect NCOCO5010Tissium · In Situ Polymerizing Peripheral Nerve Repair Device1 recall0 reports