Medical Device Recalls
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1 result found
510(K) Number: K202522 |
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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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| The Synchro SELECT Guidewires are a steerable guidewire family with a shapeable tip and are availab... | 2 | 05/31/2024 |
FEI # 3008853977 Stryker Neurovascular |
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