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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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