Medical Device Recalls
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1 result found
510(K) Number: K980927 |
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Product Description
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Recall
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FDA Recall
Posting Date |
Recalling Firm
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| Lactosorb Trauma Plating System, part numbers: 915-2100, 915-2423, 915-2113, 915-2810, 915-2418, 915... | 2 | 09/16/2008 |
FEI # 1032347 Biomet Microfixation, Inc. |
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