Medical Device Recalls
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1 result found
510(K) Number: K182425 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Stryker 1,5/1,7MM DYNAMIC MESH- STD-MEDIUM-Intended for the reconstruction, stabilization and rigid ... | 2 | 05/08/2024 |
FEI # 3002821504 Stryker Leibinger GmbH & Co. KG |
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