Medical Device Recalls
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1 result found
510(K) Number: K051385 |
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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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| ExploR Radial Head Replacement System. PN: 11-210061 LN: 243610. The stem is placed inside a poly... | 2 | 12/20/2017 |
FEI # 1825034 Zimmer Biomet, Inc. |
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