Medical Device Recalls
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1 result found
510(K) Number: K100243 |
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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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| Quintex Cervical Plating System - Screws. The Quintex Cervical Plating System is intended for the tr... | 2 | 04/25/2012 |
FEI # 2916714 Aesculap Implant Systems |
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