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U.S. Department of Health and Human Services

510(k) Premarket Notification
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21 to 27 of 27 Results
ProductCode: JDI Applicant: HOWMEDICA OSTEONICS CORP. Decision Date To: 02/07/2023
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510(K)
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trident all poly cup HOWMEDICA OSTEONICS CORP. K012026 07/18/2001
exeter hip system with v40 taper HOWMEDICA OSTEONICS CORP. K011623 06/15/2001
lfit v40 femoral head components HOWMEDICA OSTEONICS CORP. K010757 04/11/2001
modification to trident all poly cup HOWMEDICA OSTEONICS CORP. K010310 03/20/2001
trident all poly cup HOWMEDICA OSTEONICS CORP. K001956 12/11/2000
duration iv sterilization process (acetabular inserts) HOWMEDICA OSTEONICS CORP. K990849 12/20/1999
crossfire system 12 acetabular inserts HOWMEDICA OSTEONICS CORP. K993352 11/19/1999
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