Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K083782 |
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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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Knee Products: 141356 Regenerex Series-A Patella 3 Peg, 31 MM 141358 Regenerex Series-A Patella 3 ... | 2 | 05/28/2020 | Biomet, Inc. |
Regenerex Patella RGX 3 PEG SER A PATELLA 28MM RGX 3 PEG SER A PATELLA 31MM RGX 3 PEG SER A PATEL... | 2 | 04/25/2017 | Zimmer Biomet, Inc. |
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