Clearance Summary
FOSSA URETERAL OPEN LUMEN STENT received FDA 510(k) clearance under submission number K033368, sponsored by Fossa Medical, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 2003-11-26.
- Submission: K033368
- Applicant / Sponsor: Fossa Medical, Inc.
- Clearance pathway: Special
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.5130
- Decision date: 2003-11-26
Classification & Regulation
This clearance is catalogued under FDA product code EYB and 21 CFR 876.5130, within the Gastroenterology, Urology review panel as a Class II device.