Medical Device Recalls
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1 result found
510(K) Number: K033034 |
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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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VERSYS 7.5 IN BEADED FC +10 CALCAR 13.5X180MM STR +10 CALCAR 15.5X180MM STR +20 CALCAR 16.5X180M... | 2 | 03/14/2018 | Zimmer Biomet, Inc. |
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