Medical Device Recalls
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11 to 11 of 11 Results
510(K) Number: K043547 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Compress Instrument Anchor Plug Holder, stainless steel, Biomet Orthopedics, Inc., Warsaw, IN; REF 3... | 2 | 01/07/2009 | Biomet, Inc. |
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