FDA 510(k) Applications Submitted by JointVue LLC

FDA 510(k) Number Submission Date Device Name Applicant
K211656 05/28/2021 3D Echo v1.1 JointVue LLC
K172513 08/21/2017 3D Echo JointVue LLC
K173329 10/23/2017 jFit Surgical Planner JointVue LLC


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