Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K100111 |
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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 temporary devices used during the implantation of the device system: bone fixation plates an... | 2 | 11/07/2019 | Zimmer Biomet, Inc. |
NCB PERIPROSTHETIC, "NCB PP PROX FEM PLATE", Various sizes, Item Nos. 0202263009 0202263012 020226... | 2 | 11/07/2019 | Zimmer Biomet, Inc. |
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