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U.S. Department of Health and Human Services

Medical Device Recalls
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11 to 20 of 25 Results
510(K) Number: K033621
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Product Description
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FDA Recall
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MOUSE 9732721 STERILE O-ARM 10PK 2 05/09/2014 Medtronic Navigation, Inc.
PACK 9731975 TUMOR RESECTION AXIEM CR 2 05/09/2014 Medtronic Navigation, Inc.
PAK 9733497 NAV NIM-SPINE PEDICLE ACC KT 2 05/09/2014 Medtronic Navigation, Inc.
PATIENT TRACKER 9733534XOM ENT 1PK 2 05/09/2014 Medtronic Navigation, Inc.
PIN, 9733235, 100MM, STERILE, PERC REF 2 05/09/2014 Medtronic Navigation, Inc.
PIN, 9733236, 150MM, STERILE, PERC REF 2 05/09/2014 Medtronic Navigation, Inc.
SHUNT KIT 9733605 NON-INVASIVE 2 05/09/2014 Medtronic Navigation, Inc.
SPHERES 8801071 1/TRAY 12PK 2 05/09/2014 Medtronic Navigation, Inc.
SPHERES 8801075 5/TRAY 12PK 2 05/09/2014 Medtronic Navigation, Inc.
TRAJ GUIDE KIT, 9733065, BIOPSY, EXT 2 05/09/2014 Medtronic Navigation, Inc.
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