Medical Device Recalls
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1 result found
510(K) Number: K172502 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| COMP RVRS Shoulder Baseplates, including Custom Products, Item numbers 115331S 115331 115330S 115... | 2 | 11/22/2019 |
FEI # 1825034 Zimmer Biomet, Inc. |
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