Medical Device Recalls
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11 to 20 of 25 Results
510(K) Number: K022074 |
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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| PIN, 9733235, 100MM, STERILE, PERC REF | 2 | 05/09/2014 | Medtronic Navigation, Inc. |
| PATIENT TRACKER 9733534XOM ENT 1PK | 2 | 05/09/2014 | Medtronic Navigation, Inc. |
| PAK 9733497 NAV NIM-SPINE PEDICLE ACC KT | 2 | 05/09/2014 | Medtronic Navigation, Inc. |
| PACK 9731975 TUMOR RESECTION AXIEM CR | 2 | 05/09/2014 | Medtronic Navigation, Inc. |
| MOUSE 9732721 STERILE O-ARM 10PK | 2 | 05/09/2014 | Medtronic Navigation, Inc. |
| KIT, 9731427, THORACIC TACTILE PROBES | 2 | 05/09/2014 | Medtronic Navigation, Inc. |
| INSTRUMENT TRACKER 9733533XOM ENT 1PK | 2 | 05/09/2014 | Medtronic Navigation, Inc. |
| INST 9731132 KIT CR REF FRAME DRIVER 5PK | 2 | 05/09/2014 | Medtronic Navigation, Inc. |
| ENT PRGM 9734636 ADD FUSION NAV AxiEM | 2 | 05/09/2014 | Medtronic Navigation, Inc. |
| DRAPE 9732722 TUBE STERILE O-ARM 20PK | 2 | 05/09/2014 | Medtronic Navigation, Inc. |
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