Medical Device Recalls
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1 result found
510(K) Number: K122138 |
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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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Flixene IFG with Assisted Delivery Intended for use in arterial vascular reconstruction, segmental... | 2 | 09/30/2013 | Atrium Medical Corporation |
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