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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