Medical Device Recalls
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1 result found
510(K) Number: K071420 |
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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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Drill Guide - Chameleon FacetFuse Fixation System, Model: 11-00028 Rev. A FacetFuse Drill Guides ... | 2 | 08/02/2013 | SpineFrontier, Inc. |
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