Medical Device Recalls
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1 result found
510(K) Number: K141187 |
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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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IMPIX ALIF S/A, REF number B15241415; intervertebral fusion device - lumbar | 2 | 08/24/2023 | Medicrea International |
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