Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K173057 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| NexGen Precoat Stemmed Tibial Plate Size 5 | 2 | 07/05/2023 |
FEI # 1000220733 Zimmer, Inc. |
| Various Knee Systems for knee joint arthroplasty, knee prosthesis, Item Nos. 00522000100 0052200020... | 2 | 11/07/2019 |
FEI # 1000220733 Zimmer Biomet, Inc. |
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