Medical Device Recalls
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1 result found
510(K) Number: K211769 |
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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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OneLIF Torque Limiting Adapter, AO to 1/4 SQ, 2.25Nm Limit, Catalog #015-010-0000, a component of No... | 2 | 11/17/2022 | Novapproach Spine LLC |
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