Medical Device Recalls
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1 result found
510(K) Number: K071577 |
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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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| Lactosorb Pectus Stabilizer, model number: 01-3805. Distributed and Manufactured by : Biomet Microfi... | 2 | 05/27/2009 |
FEI # 1032347 Biomet Microfixation, Inc. |
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