Medical Device Recalls
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1 result found
510(K) Number: K192122 |
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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 Trak 21 Microcatheter, REF: 90338. TREVO NXT 3X32+TRAK21 2-PACK - CE, REF: 91412; TREVO NX... | 2 | 07/15/2022 | Stryker Neurovascular |
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