Medical Device Recalls
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1 result found
510(K) Number: K972233 |
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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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STRYKER WEDGE INTERFERENCE SCREW SYSTEM, ACL Interface Screw, 9MM X 25MM, Model 0234010056, labeled ... | 2 | 03/02/2018 | Stryker Corporation |
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