Medical Device Recalls
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1 result found
510(K) Number: K081023 |
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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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Evolis-Femoral Sizer Posterior Reference The femoral sizer posterior reference is a manual orthop... | 2 | 06/26/2015 | Medacta Usa Inc |
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