Medical Device Recalls
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1 result found
510(K) Number: K973124 |
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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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Various Hip Joint Replacement Systems, Item Nos. 00151504232 00151504432 00151504636 00151504836 ... | 2 | 11/07/2019 | Zimmer Biomet, Inc. |
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