Clearance Summary
Solon received FDA 510(k) clearance under submission number K221766, sponsored by Lmg Lasers Comercio, Importacao E Exportacao Ltda. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2024-01-05.
- Submission: K221766
- Applicant / Sponsor: Lmg Lasers Comercio, Importacao E Exportacao Ltda
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.4810
- Decision date: 2024-01-05
Classification & Regulation
This clearance is catalogued under FDA product code GEX and 21 CFR 878.4810, within the General, Plastic Surgery review panel as a Class II device.