Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K212027 |
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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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Medtronic TurboHawk Plus Directional Atherectomy System 6F, Small Vessel, Catalog number THP-S. For... | 1 | 03/07/2022 | ev3 Inc. |
Medtronic TurboHawk Plus Directional Atherectomy System 6F, Multi-vessel, Catalog number THP-M. For ... | 1 | 03/07/2022 | ev3 Inc. |
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