Medical Device Recalls
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81 to 81 of 81 Results
510(K) Number: K072642 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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3i Custom # 5753, OSCM2913, 2.9MMX 3.4MM X 13MM, OSSEOTITE CUSTOM, MICROMINI IMPLANT, LOT # 470258, ... | 2 | 09/22/2009 | Biomet 3i, LLC |
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