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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: K022074
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Product Description
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Recall
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FDA Recall
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TRAJ GUIDE KIT, 9733066, BIOPSY, INT 2 05/09/2014 Medtronic Navigation, Inc.
TUMOR RES. PACK 9733553 AxiEM S.M. 2 05/09/2014 Medtronic Navigation, Inc.
TUMOR RESECTION KIT 9733607 NON-INVASIVE 2 05/09/2014 Medtronic Navigation, Inc.
TUMOR RESECTION KIT 9733608 SKULL MOUNT 2 05/09/2014 Medtronic Navigation, Inc.
BIOPSY NEEDLE KIT, 9733068, PASSIVE 2 05/09/2014 Medtronic Navigation, Inc.
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