Medical Device Recalls
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1 result found
510(K) Number: K964509 |
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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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| 00720504022 ACETAB.CUPW/SH,0DEG,22MMX40MM 00720504222 ACETAB.CUPW/SH,0DEG,22MMX42MM 00720504622 ... | 2 | 06/10/2016 |
FEI # 3005751028 Zimmer Trabecular Metal Technology, Inc. |
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