Clearance Summary
MODEL 3587A RESUME EPIDURAL LEAD received FDA 510(k) clearance under submission number K884948, sponsored by Medtronic Vascular. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 1989-01-17.
- Submission: K884948
- Applicant / Sponsor: Medtronic Vascular
- Clearance pathway: Traditional
- Review panel: Neurology
- Device class: Class II
- Regulation citation: 21 CFR 882.5880
- Decision date: 1989-01-17
Classification & Regulation
This clearance is catalogued under FDA product code GZB and 21 CFR 882.5880, within the Neurology review panel as a Class II device.