Medical Device Recalls
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1 result found
510(K) Number: K171715 |
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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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HammerTube Implant, 2.75mm, 10® Cannulated (Sterile) | 2 | 07/27/2022 | Paragon 28, Inc. |
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