Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K213530 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Nextra Cannulated Hammertoe Standard Instrument Kit-indicated for small bone reconstruction limited ... | 2 | 03/09/2022 | Nextremity Solutions |
| Nextra CH Cannulated Hammertoe Mini Instrument Kit-indicated for small bone reconstruction limited t... | 2 | 03/09/2022 | Nextremity Solutions |
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