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U.S. Department of Health and Human Services

510(k) Premarket Notification
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11 to 20 of 27 Results
ProductCode: JDI Applicant: HOWMEDICA OSTEONICS CORP. Decision Date To: 02/07/2023
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Export all 27 Records to ExcelExport to Excel | Download Files | More About 510(k)
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modification to trident all poly cup HOWMEDICA OSTEONICS CORP. K010310 03/20/2001
modification to: restoration modular system HOWMEDICA OSTEONICS CORP. K050138 03/21/2005
omnifit hfx hip stem series HOWMEDICA OSTEONICS CORP. K031744 08/08/2003
super eon plus femoral stems HOWMEDICA OSTEONICS CORP. K020989 04/26/2002
trident all poly cup HOWMEDICA OSTEONICS CORP. K001956 12/11/2000
trident all poly cup HOWMEDICA OSTEONICS CORP. K012026 07/18/2001
trident screw hole plug and trident bone spike HOWMEDICA OSTEONICS CORP. K022799 11/21/2002
restoration® modular hip system Howmedica Osteonics Corp. (aka Stryker Orthopaedics) K193233 05/27/2020
trident ii acetabular system Howmedica Osteonics Corp. aka Stryker Orthopaedics K191358 10/24/2019
trident® ii acetabular system Howmedica Osteonics Corp. aka Stryker Orthopaedics K171768 10/02/2017
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