K241917
- 510(k) number
- K241917
- Device name
- EARP Nerve Cuff Electrode
- Applicant
- Retropsoas Technologies, LLC MO · US
- Product code
- ETN — Stimulator, Nerve
- Decision date
- 2024-07-31
- Date received
- 2024-07-01
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Ear, Nose, Throat
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K241917.pdf
Official FDA record: K241917
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.