Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K113260 |
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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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Trevo XP ProVue System kit containing 1) Trevo XP ProVue Retriever, 4x20mm and 2) Trevo Pro18 Microc... | 2 | 01/14/2018 | Stryker Neurovascular |
Trevo(TM) XP ProVue Procedure Pack, TREVO(TM) XP PROVUE RETRIEVER, 6 mm, 25 mm, .Excelsior(TM) XT-27... | 2 | 12/05/2017 | Stryker Neurovascular |
Stroke Fast Pack(TM), Trevo(TM) XP, TREVO(TM) XP PROVUE RETRIEVER, 6 mm, 25 mm; Excelsior(TM) XT-27(... | 2 | 12/05/2017 | Stryker Neurovascular |
Stroke Fast Pack(TM), Trevo(TM) XP, TREVO(TM) XP PROVUE RETRIEVER, 4 mm, 20 mm, ; Trevo(TM) Pro 18, ... | 2 | 12/05/2017 | Stryker Neurovascular |
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