Clearance Summary
SURGIMOTOR received FDA 510(k) clearance under submission number K954470, sponsored by W.O.M. World of Medicine GmbH. 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 1995-12-08.
- Submission: K954470
- Applicant / Sponsor: W.O.M. World of Medicine GmbH
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class I
- Regulation citation: 21 CFR 878.4820
- Decision date: 1995-12-08
Classification & Regulation
This clearance is catalogued under FDA product code GEY and 21 CFR 878.4820, within the General, Plastic Surgery review panel as a Class I device.