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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 2 of 2 Results
510(K) Number: K083798
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Product Description
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Recall
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FDA Recall
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IMPIX TLIF, REF numbers: a) B15130607S, b) B15130609S, c) B15130611S, d) B15130613S, e) B... 2 08/24/2023 Medicrea International
IMPIX ALIF, REF numbers: a) B15111209, b) B15111212, c) B15111409, d) B15111412; interve... 2 08/24/2023 Medicrea International
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