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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