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FDA 510(k) Applications Submitted by Julia Bally
FDA 510(k) Number
Submission Date
Device Name
Applicant
K240418
02/13/2024
Stryker Orthopaedics Hip Systems Labeling Update
Howmedica Osteonics Corp. dba Stryker Orthopaedics
K241716
06/14/2024
Global Modular Replacement System, Modular Replacement System, Modular Rotating Hinge Knee Component
Howmedica Osteonics Corp. dba Stryker Orthopaedics
K233498
10/31/2023
Stryker Orthopaedics Hip Systems Labeling Update
Howmedica Osteonics Corp. dba Stryker Orthopaedics
K243784
12/09/2024
Stryker Orthopaedics Hip Devices Labeling Update
Howmedica Osteonics Corp. dba Stryker Orthopaedics
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