Medical Device Recalls
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1 result found
510(K) Number: K202224 |
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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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SpaceOAR System, UPN SO-1010, SO-2101, SO-3101, and SO-4101. Used to temporarily position the anter... | 2 | 04/25/2022 | Boston Scientific Corporation |
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