FDA 510(k) Applications Submitted by Wei Chun Chang

FDA 510(k) Number Submission Date Device Name Applicant
K163506 12/14/2016 CoalesceÖ (-Straight, -Convex, -Crescent, -Lateral, -Anterior, or -Oblique) Lumbar Interbody Fusion System Vertera, Inc.
K241775 06/20/2024 XeliteMed VertehighFix High Viscosity Spinal Bone Cement Xelite Biomed Ltd.
K243537 11/15/2024 XeliteMed VertehighFix High Viscosity Spinal Bone Cement System XELITE BIOMED LTD.


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