FDA 510(k) Applications Submitted by Tyler Kulcsar

FDA 510(k) Number Submission Date Device Name Applicant
K230653 03/09/2023 Smith & Nephew, Inc. ANTHEM Total Knee System, Genesis Uni Knee System, JOURNEY BCS and II Knee Systems, JOURNEY II CR Knee System, JOURNEY II Uni Knee System, Journey II UK Knee System, JOURNEY II XR Bi-Cruciate Retaining Knee System, JOURNEY PFJ System, Smith & Nephew, Inc.


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