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U.S. Department of Health and Human Services

Medical Device Recalls
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1 result found
510(K) Number: K170359
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Corin Trinity Dual Mobility, Size 4, Dual Mobility CoCr Liner, REF 321.04.540, Sterile, and Corin Du... 2 09/30/2021 FEI # 3002806725
Corin Ltd
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