Clearance Summary
SILICONE INSTRUMENT SHODS received FDA 510(k) clearance under submission number K895591, sponsored by Key Surgical, 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 1989-10-20.
- Submission: K895591
- Applicant / Sponsor: Key Surgical, Inc.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class I
- Regulation citation: 21 CFR 878.4800
- Decision date: 1989-10-20
Classification & Regulation
This clearance is catalogued under FDA product code GDJ and 21 CFR 878.4800, within the General, Plastic Surgery review panel as a Class I device.