Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K181083 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Stryker, Omega 4.75 mm,. PEEK Knotless Anchor System, Single, REF 3910-500-471, UDI 07613327464818, ... | 2 | 03/02/2020 | Stryker Corporation |
| Stryker, Omega 4.75 mm,. PEEK Knotless Anchor System, Double-Double, REF 3910-500-472, UDI 076133274... | 2 | 03/02/2020 | Stryker Corporation |
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