FDA 510(k) Applications Submitted by DAVID KOPPERDAHL

FDA 510(k) Number Submission Date Device Name Applicant
K220402 02/11/2022 VirtuOst O.N. Diagnostics
K171435 05/15/2017 VirtuOst Vertebral Fracture Assessment O.N. Diagnostics, LLC.
K113725 12/19/2011 VIRTUOST O.N. DIAGNOSTICS


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