Medical Device Recalls
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1 result found
510(K) Number: K113695 |
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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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| NUVASIVE PRECICE UNYTE System (Humerus and Tibia): PRECICE Trauma Nail System/PRECICE Unyte-Humer... | 2 | 04/05/2021 |
FEI # 3006179046 Nuvasive Specialized Orthopedics Inc |
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