Medical Device Recalls
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1 result found
510(K) Number: K993418 |
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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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Stryker brand GDC VORTX 2MM X 3MM, Catalog Number: M00335302340; Product is manufactured by Stryker... | 2 | 12/13/2013 | Stryker Neurovascular |
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