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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K936008
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LARGE PRIMARY REV.TIB.INSERT- DURACON Intended for knee replacement Product Number: 6637-4... 2 01/31/2024 Howmedica Osteonics Corp.
PRIMARY REV.TIB.INSERT-DURACON Intended for knee replacement. Product Number: 6637-4-031 2 01/31/2024 Howmedica Osteonics Corp.
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