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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: K962082
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DURACON XL ANGLED TIB INS 11/14MM C-M064-1-300 SELF-PRESSURIZING GLENOID SIZE 8 C-M062-6-8... 2 09/16/2026 FEI # 3003070421
Howmedica Osteonics Corp.
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