Medical Device Recalls
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1 result found
510(K) Number: K993943 |
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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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| HA Hip Stem, cementless | 2 | 07/22/2004 |
FEI # 1000116912 Encore Medical, Lp |
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