Clearance Summary
Fraxis received FDA 510(k) clearance under submission number K172096, sponsored by Ilooda Co,., 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 2017-08-09.
- Submission: K172096
- Applicant / Sponsor: Ilooda Co,., Ltd.
- Clearance pathway: Special
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.4810
- Decision date: 2017-08-09
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.