Medical Device Recalls
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1 result found
510(K) Number: K973524 |
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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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ADVANCE TIBIAL WEDGE AUGMENT, REF KTAG-W315, SIZE 3/2+, Thickness 15 DEG, SURFACE NON-POROUS, 1 EACH... | 2 | 03/31/2010 | Wright Medical Technology Inc |
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