Medical Device Recalls
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1 result found
510(K) Number: K162732 |
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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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Alteon HA Femoral Stem, Press-Fit, Extended Offset, Cementless, HA Coated, Collared, Size 5 All... | 2 | 01/18/2018 | Exactech, Inc. |
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