Medical Device Recalls
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1 result found
510(K) Number: K141407 |
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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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Vanguard XP Knee System Porous Femoral Component various sizes and orientation a total knee replac... | 2 | 03/25/2016 | Biomet, Inc. |
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