FDA 510(k) Applications Submitted by Retropsoas Technologies, LLC
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K241917 | 07/01/2024 | EARP Nerve Cuff Electrode | Retropsoas Technologies, LLC |
| K242457 | 08/19/2024 | EARP Interbody System | Retropsoas Technologies, LLC |
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