EARP Nerve Cuff Electrode
FDA 510(k) clearance K241917 · decided 2024-07-31
Clearance details
- K-number
- K241917
- Device name
- EARP Nerve Cuff Electrode
- Applicant
- Retropsoas Technologies, LLC
- Decision
- Substantially Equivalent
- Date received
- 2024-07-01
- Decision date
- 2024-07-31
- Days to decision
- 30 days
- Clearance type
- Special
- Product code
- ETN
- Device class
- 2
- Regulation number
- 874.1820
- Medical specialty
- Ear, Nose, Throat
- Advisory committee
- Ear, Nose, Throat
- Location
- Frontenac, MO, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.