Clearance Summary
SCOTTS SURGICAL RETRACTOR AND ELASTIC received FDA 510(k) clearance under submission number K791665, sponsored by Lone Star 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 1979-09-19.
- Submission: K791665
- Applicant / Sponsor: Lone Star Medical Products, Inc.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class I
- Regulation citation: 21 CFR 878.4800
- Decision date: 1979-09-19
Classification & Regulation
This clearance is catalogued under FDA product code GAD and 21 CFR 878.4800, within the General, Plastic Surgery review panel as a Class I device.