Medical Device Recalls
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1 result found
510(K) Number: K211002 |
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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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Grappler Suture Anchor, Titanium, 3.0 x 10mm, Sterile Kit, REF: P44-110-3010-SK, for use within the ... | 2 | 09/22/2022 | Paragon 28, Inc. |
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