FDA 510(k) Applications Submitted by Margaret Crowe Klippel

FDA 510(k) Number Submission Date Device Name Applicant
K190402 02/19/2019 Triathlon Total Knee System-Additional Components Stryker Orthopaedics (aka Howmedica Osteonics Corp.)
K220838 03/22/2022 Artisan Bone Plug, Universal Cement Restrictor Howmedica Osteonics, dba Stryker Orthopaedics
K222056 07/12/2022 Global Modular Replacement System, Modular Replacement System, Modular Rotating Hinge Knee Howmedica Osteonics Corp., dba Stryker Orthopaedics
K212187 07/13/2021 Restoration« Modular Hip System Howmedica Osteonics Corp., dba Stryker Orthopaedics
K202016 07/21/2020 Dall-Miles« Cable System Howmedica Osteonics Corp., dba Stryker Orthopaedics
K172326 08/01/2017 Triathlon Total Knee System, Triathlon PKR System, Restoris MCK Knee System Stryker Orthopaedics
K222632 08/31/2022 UHR Bipolar Implants, Restoration GAP II Implants Howmedica Osteonics Corp., dba Stryker Orthopaedics
K223069 09/30/2022 Modular Rotating Hinge Knee Systems and Compatible Components Howmedica Osteonics Corp. dba Stryker Orthopaedics
K153345 11/19/2015 Stryker Orthopaedics Hip Systems Labeling Update STRYKER ORTHOPAEDICS
K143393 11/26/2014 Triathlon Tritanium Cone Augments STRYKER ORTHOPAEDICS
K173849 12/19/2017 Triathlon Total Knee System Stryker Orthopaedics


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