Medical Device Recalls
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1 to 10 of 25 Results
510(K) Number: K033621 |
Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| UPGRD PRGM 9734638 ADD AxiEM NAVIGATION | 2 | 05/09/2014 | Medtronic Navigation, Inc. |
| TUMOR RESECTION KIT 9733608 SKULL MOUNT | 2 | 05/09/2014 | Medtronic Navigation, Inc. |
| TUMOR RESECTION KIT 9733607 NON-INVASIVE | 2 | 05/09/2014 | Medtronic Navigation, Inc. |
| TUMOR RES. PACK 9733553 AxiEM S.M. | 2 | 05/09/2014 | Medtronic Navigation, Inc. |
| TRAJ GUIDE KIT, 9733066, BIOPSY, INT | 2 | 05/09/2014 | Medtronic Navigation, Inc. |
| TRAJ GUIDE KIT, 9733065, BIOPSY, EXT | 2 | 05/09/2014 | Medtronic Navigation, Inc. |
| SPHERES 8801075 5/TRAY 12PK | 2 | 05/09/2014 | Medtronic Navigation, Inc. |
| SPHERES 8801071 1/TRAY 12PK | 2 | 05/09/2014 | Medtronic Navigation, Inc. |
| SHUNT KIT 9733605 NON-INVASIVE | 2 | 05/09/2014 | Medtronic Navigation, Inc. |
| PIN, 9733236, 150MM, STERILE, PERC REF | 2 | 05/09/2014 | Medtronic Navigation, Inc. |
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