Clearance Summary
INTRASTENT LD (LARGE DIAMETER) STENT received FDA 510(k) clearance under submission number K020528, sponsored by Sulzer Intratherapeutics, 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 2002-04-16.
- Submission: K020528
- Applicant / Sponsor: Sulzer Intratherapeutics, Inc.
- Clearance pathway: Special
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.5010
- Decision date: 2002-04-16
Classification & Regulation
This clearance is catalogued under FDA product code FGE and 21 CFR 876.5010, within the Gastroenterology, Urology review panel as a Class II device.