Clearance Summary
SAFE-STEER GUIDE WIRE SYSTEM received FDA 510(k) clearance under submission number K011986, sponsored by Intra Luminal Therapeutics, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2002-04-03.
- Submission: K011986
- Applicant / Sponsor: Intra Luminal Therapeutics, Inc.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.1330
- Decision date: 2002-04-03
Classification & Regulation
This clearance is catalogued under FDA product code DQX and 21 CFR 870.1330, within the Cardiovascular review panel as a Class II device.