Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K980486 |
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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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00720504022 ACETAB.CUPW/SH,0DEG,22MMX40MM 00720504222 ACETAB.CUPW/SH,0DEG,22MMX42MM 00720504622 ... | 2 | 06/10/2016 | Zimmer Trabecular Metal Technology, Inc. |
REV. SHELL LINER 0D 28X48 00700504828 REV. SHELL LINER 10D 28X50 00701005028 REV. SHELL LINER... | 2 | 06/10/2016 | Zimmer Trabecular Metal Technology, Inc. |
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