Clearance Summary
MEDUS GMBH received FDA 510(k) clearance under submission number K853153, sponsored by Corkes Medical Co.. 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 1985-08-07.
- Submission: K853153
- Applicant / Sponsor: Corkes Medical Co.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class I
- Regulation citation: 21 CFR 878.4800
- Decision date: 1985-08-07
Classification & Regulation
This clearance is catalogued under FDA product code GEN and 21 CFR 878.4800, within the General, Plastic Surgery review panel as a Class I device.