Clearance Summary
FINESSE 3RD GENERATION (MODELS FINESSE+ AND FINESSEII+) received FDA 510(k) clearance under submission number K123310, sponsored by Utah Medical Products, Inc.. 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 2013-01-23.
- Submission: K123310
- Applicant / Sponsor: Utah Medical Products, Inc.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.4400
- Decision date: 2013-01-23
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.