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U.S. Department of Health and Human Services

Medical Device Recalls
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21 to 25 of 25 Results
510(K) Number: K033621
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Product Description
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FDA Recall
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DISP 9730951 STRL SPHERE, 5PK INSERT 2 05/09/2014 Medtronic Navigation, Inc.
DISP 9730950 STRL SPHERE, 1 PK INSERT 2 05/09/2014 Medtronic Navigation, Inc.
BIT 9733516 2.9mm DRILL STERILE 2 05/09/2014 Medtronic Navigation, Inc.
BIOPSY NEEDLE KIT, 9733068, PASSIVE 2 05/09/2014 Medtronic Navigation, Inc.
BAG 9732315 MOUSE STERILE 15 PK 2 05/09/2014 Medtronic Navigation, Inc.
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