Medtronic Cardiac Surgery Technologies
4 FDA 510(k) clearances · Recalling firm
◉ Watch Medtronic Cardiac Surgery Technologies
| Record | Firm | Date |
|---|---|---|
| VNUS Medical U-CLIP Removal Tool, UREM1860, is intended for the removal of U-Clip anastomo recall (Z-1609-2008) | Medtronic Cardiac Surgery Technologies | 2008-09-16 |
| Medtronic Cardioblate Gemini-s, model 49260. Surgical Ablation Device. Sterilized using Et recall (Z-0727-2008) | Medtronic Cardiac Surgery Technologies | 2008-02-02 |
| Medtronic U-CLIP Anastomotic Device Removal Tool, model REM1860FW. The U-Clip Anastomotic recall (Z-0968-2007) | Medtronic Cardiac Surgery Technologies | 2007-06-27 |
| Medtronic SPYDER Anastomotic Device. Sterilized using irradiation. Do not Reuse. Nonpyroge recall (Z-0763-06) | Medtronic Cardiac Surgery Technologies | 2006-04-13 |
Track Medtronic Cardiac Surgery Technologies automatically
Every clearance here is in the API, with alerts when new ones post.