Clearance Summary
MEDART 620 received FDA 510(k) clearance under submission number K120573, sponsored by Medart 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 2012-06-13.
- Submission: K120573
- Applicant / Sponsor: Medart A/S
- Clearance pathway: Special
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.4810
- Decision date: 2012-06-13
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.