Medical Device Recalls
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1 result found
510(K) Number: K991031 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Medtronic Sofamor Danek COLORADO 2" SPINAL SYSTEM Break-Off Nut, non-sterile, RX; Catalog Number 863... | 2 | 02/07/2008 |
FEI # 1824199 Warsaw Orthopedic, Inc. dba Medtronic SOFAMOR DANEK |
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