Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K151314 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Stryker CinchLock Flex Knotless Anchor with Inserter and Suture, REF CAT02643, Sterile EO, Rx Only M... | 2 | 03/12/2025 |
FEI # 2936485 Stryker Corporation |
| CinchLock Flex Knotless Anchor with Inserter; Model number CAT02643; Orthopedic: The Pivot Cinc... | 2 | 05/10/2016 |
FEI # 2936485 Stryker Corporation |
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