Clearance Summary
NEUROMARK System (NMK00301) received FDA 510(k) clearance under submission number K261833, sponsored by Neurent Medical , Ltd.. The device was reviewed via the Special premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2026-06-16.
- Submission: K261833
- Applicant / Sponsor: Neurent Medical , Ltd.
- Clearance pathway: Special
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.4400
- Decision date: 2026-06-16
Classification & Regulation
This clearance is catalogued under FDA product code GEI and 21 CFR 878.4400, within the General, Plastic Surgery review panel as a Class II device.