Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K161592 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Persona Partial Knee spacer block instruments; (1) 8mm block, Model Number: 42-5399-035-08; (2) 9mm ... | 2 | 03/28/2018 |
FEI # 1825034 Zimmer Biomet, Inc. |
| Persona Partial Knee System, Size 8, Finishing Guide | 2 | 01/14/2018 |
FEI # 1825034 Zimmer Biomet, Inc. |
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