Medical Device Recalls
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1 result found
510(K) Number: K110197 |
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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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Gibralt Spine System Polyaxial Screw Intended to promote fusion of the cervical spine, and the th... | 2 | 03/18/2014 | Exactech, Inc. |
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