Clearance Summary
FRONTAL SINUS TREPHINATION CANNULA received FDA 510(k) clearance under submission number K994262, sponsored by Xomed, 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 2000-02-08.
- Submission: K994262
- Applicant / Sponsor: Xomed, Inc.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class I
- Regulation citation: 21 CFR 878.4800
- Decision date: 2000-02-08
Classification & Regulation
This clearance is catalogued under FDA product code KAM and 21 CFR 878.4800, within the General, Plastic Surgery review panel as a Class I device.