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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: 11/27/2021
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Export all 27 Records to ExcelExport to Excel | Download Files | More About 510(k)
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restoration modular 115mm conical distal stem Howmedica Osteonics Corp., dba Stryker Orthopaedics K213129 12/21/2021
omnifit hfx hip stem series HOWMEDICA OSTEONICS CORP. K031744 08/08/2003
modification to: restoration modular system HOWMEDICA OSTEONICS CORP. K050138 03/21/2005
modification to trident all poly cup HOWMEDICA OSTEONICS CORP. K010310 03/20/2001
modification to restoration modular system HOWMEDICA OSTEONICS CORP. K040734 08/25/2004
lfit v40 femoral head components HOWMEDICA OSTEONICS CORP. K010757 04/11/2001
global modular replacement system, modular replacement system, modular rotating hinge knee Howmedica Osteonics Corp., dba Stryker Orthopaedics K222056 01/26/2023
global modular replacement system (gmrs) HOWMEDICA OSTEONICS CORP. K023087 12/16/2002
exeter® x3® rimfit® cup Howmedica Osteonics Corp., dba Stryker Orthopaedics K213701 02/01/2022
exeter hip system with v40 taper HOWMEDICA OSTEONICS CORP. K011623 06/15/2001
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