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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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