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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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Export all 27 Records to ExcelExport to Excel | Download Files | More About 510(k)
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trident® ii tritanium® acetabular shells and 6.5 mm low profile hex screws Howmedica Osteonics Corp. aka Stryker Orthopaedics K161569 10/14/2016
acetabular dome hole plug Howmedica Osteonics Corp., dba Stryker Orthopaedics K220376 03/09/2022
exeter® x3® rimfit® cup Howmedica Osteonics Corp., dba Stryker Orthopaedics K213701 02/01/2022
global modular replacement system, modular replacement system, modular rotating hinge knee Howmedica Osteonics Corp., dba Stryker Orthopaedics K222056 01/26/2023
restoration modular 115mm conical distal stem Howmedica Osteonics Corp., dba Stryker Orthopaedics K213129 12/21/2021
restoration® modular hip system Howmedica Osteonics Corp., dba Stryker Orthopaedics K212187 03/01/2022
uhr bipolar implants, restoration gap ii implants Howmedica Osteonics Corp., dba Stryker Orthopaedics K222632 10/21/2022
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