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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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