Medical Device Recalls
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1 result found
510(K) Number: K170923 |
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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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P28 JAWS Nitinol Staple System kits are designed for use in an osteotomy, arthrodesis and fragment f... | 2 | 06/20/2018 | Paragon 28, Inc. |
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