Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K051320 |
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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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Satellite Spinal System Primary User Group Reference Guide, 8 1/2 by 11 inch plastic binder, Medtron... | 2 | 12/22/2007 | Medtronic Sofamor Danek USA Inc |
8mm SATELLITE® Sphere CoCr contained in a SATELLITE® Spinal System (internal fixation device-verte... | 2 | 06/08/2006 | Medtronic Sofamor Danek USA Inc |
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