Medical Device Recalls
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1 result found
510(K) Number: K880155 |
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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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FEM PRC LT M/RT L SML FEM PRC RT M/LT L SML FEM PRC LT M/RT L SML+ FEM ... | 2 | 03/14/2018 | Zimmer Biomet, Inc. |
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