FDA 510(k) Applications Submitted by SCOTT COLERIDGE

FDA 510(k) Number Submission Date Device Name Applicant
K221010 04/05/2022 Intra.Ox 2.0 Handheld Tissue Oximeter ViOptix, Inc.
K191676 06/24/2019 Intra.Ox 2.0 Handheld Tissue Oximeter ViOptix, Inc.
K153057 10/21/2015 FitRiteÖ Total Hip Arthroplasty System EXCERA ORTHOPEDICS, INC.


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