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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K990214
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Product Description
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Recall
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FDA Recall
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Left Long Tactile Probe, Part #962009S, Medtronic Navigation, Louisville, CO 80027. Trackable ha... 2 03/08/2012 FEI # 1000517638
Medtronic Navigation, Inc.
Right Long Tactile Probe, Part #962011S, Medtronic Navigation, Louisville, CO 80027. Trackable h... 2 03/08/2012 FEI # 1000517638
Medtronic Navigation, Inc.
Probe, Tactile, Left, ASM, Long, Part #962009S, Medtronic Navigation, Louisville, CO 80027. ... 2 10/03/2011 FEI # 1000517638
Medtronic Navigation, Inc
Probe, Tactile, Right, ASM, Long, Part #962011S, Medtronic Navigation, Louisville, CO 80027. ... 2 10/03/2011 FEI # 1000517638
Medtronic Navigation, Inc
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