Medical Device Recalls
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1 result found
510(K) Number: K003429 |
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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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Mallory/Head Primary Hip System; Size 11, 160 mm, Lateralized Femoral Stem; Ti-6Al-4V; Porous Plasma... | 3 | 06/11/2015 | Biomet, Inc. |
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