Medical Device Recalls
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1 result found
510(K) Number: K120990 |
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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 Knee Systems, Item Nos. 32855411838 32855411840 32855411842 32855411843 32855420307 328... | 2 | 11/07/2019 | Zimmer Biomet, Inc. |
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