Clearance Summary
VOLISTA 400; VOLISTA 600 received FDA 510(k) clearance under submission number K130513, sponsored by Maquet S.A.S.. 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 2013-05-08.
- Submission: K130513
- Applicant / Sponsor: Maquet S.A.S.
- Clearance pathway: Special
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.4580
- Decision date: 2013-05-08
Classification & Regulation
This clearance is catalogued under FDA product code FTD and 21 CFR 878.4580, within the General, Plastic Surgery review panel as a Class II device.