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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