Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K021980 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Fix pins associated with Stealth Station Treatment Guidance Platform | 2 | 12/17/2003 | Medtronic Surgical Navigation Tech, Inc |
Medtronic Orthopedic Dovetail Clamp, REF 9730289, Medtronic Navigation, Louisville, CO 80027. In ... | 2 | 03/03/2010 | Medtronic Navigation, Inc |
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