Clearance Summary
JAIN GRAFT ASSIST received FDA 510(k) clearance under submission number K904536, sponsored by Jain Surgical Equipment, 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 1990-11-29.
- Submission: K904536
- Applicant / Sponsor: Jain Surgical Equipment, Inc.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class I
- Regulation citation: 21 CFR 878.4800
- Decision date: 1990-11-29
Classification & Regulation
This clearance is catalogued under FDA product code GCZ and 21 CFR 878.4800, within the General, Plastic Surgery review panel as a Class I device.