Medical Device Recalls
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1 result found
510(K) Number: K173352 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Trevo XP ProVue Retriever 4 x 20, Catalog: 90182 Trevo XP ProVue Retriever 3 x 20, Catalog: 90183 ... | 2 | 05/28/2024 |
FEI # 3008853977 Stryker Neurovascular |
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