Medical Device Recalls
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1 result found
510(K) Number: K942479 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Biomet Integral Centralizer Hip System, Lateralized Femoral Stem (Co-Cr-Mo), 9mm, 11mm, 13mm, 15mm,... | 2 | 01/13/2016 | Biomet, Inc. |
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