Medical Device Recalls
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1 result found
510(K) Number: K911902 |
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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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The Oxford Partial Knee; Oxford Knee Resection Procedure 3 Pack CEMENTED For use with Stryker Syste... | 2 | 04/17/2013 | Synvasive Technology Inc |
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