Medical Device Recalls
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1 to 10 of 28 Results
510(K) Number: K001284 |
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
AxiEM EM Knee Kit, and associated workstation. | 3 | 04/07/2006 | Medtronic Navigation, Inc |
BAG 9732315 MOUSE STERILE 15 PK | 2 | 05/09/2014 | Medtronic Navigation, Inc. |
BIOPSY NEEDLE KIT, 9733068, PASSIVE | 2 | 05/09/2014 | Medtronic Navigation, Inc. |
BIT 9733516 2.9mm DRILL STERILE | 2 | 05/09/2014 | Medtronic Navigation, Inc. |
DISP 9730950 STRL SPHERE, 1 PK INSERT | 2 | 05/09/2014 | Medtronic Navigation, Inc. |
DISP 9730951 STRL SPHERE, 5PK INSERT | 2 | 05/09/2014 | Medtronic Navigation, Inc. |
DRAPE 9732722 TUBE STERILE O-ARM 20PK | 2 | 05/09/2014 | Medtronic Navigation, Inc. |
ENT PRGM 9734636 ADD FUSION NAV AxiEM | 2 | 05/09/2014 | Medtronic Navigation, Inc. |
Fusion ENT Application. The software application is sent in CD format with an IFU, wrapped in plasti... | 2 | 08/02/2016 | Medtronic Navigation, Inc. |
INST 9731132 KIT CR REF FRAME DRIVER 5PK | 2 | 05/09/2014 | Medtronic Navigation, Inc. |
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