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FDA 510(k) Applications Submitted by Subchondral Solutions, Inc.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K220901
03/28/2022
S-Core Implant System
Subchondral Solutions, Inc.
K191995
07/26/2019
S4 Screw System
Subchondral Solutions, Inc.
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