Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K081465 |
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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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Axium Detachable Coil System QC-7-30-Helix The ev3 Axium Detachable Coil System is indicated for... | 3 | 01/26/2012 | Micro Therapeutics Inc, dba ev3 Neurovascular |
Axium Detachable Coil System QC-2-1-Helix The ev3 Axium Detachable Coil System is indicated for ... | 3 | 01/26/2012 | Micro Therapeutics Inc, dba ev3 Neurovascular |
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