FDA 510(k) Applications Submitted by Howmedica Osteonics Corp., dba Stryker Orthopaedics
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K213129 |
09/27/2021 |
Restoration Modular 115mm Conical Distal Stem |
Howmedica Osteonics Corp., dba Stryker Orthopaedics |
K220376 |
02/10/2022 |
Acetabular Dome Hole Plug |
Howmedica Osteonics Corp., dba Stryker Orthopaedics |
K213701 |
11/24/2021 |
Exeter« X3« RimFit« Cup |
Howmedica Osteonics Corp., 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 |
K222632 |
08/31/2022 |
UHR Bipolar Implants, Restoration GAP II Implants |
Howmedica Osteonics Corp., dba Stryker Orthopaedics |
K211303 |
04/29/2021 |
Avon Patello-femoral Joint Prosthesis |
Howmedica Osteonics Corp., dba Stryker Orthopaedics |
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