Clearance Summary
MODEL 3873 1* 8 AND MODEL 3874 1* 8 COMPACT TEST STIMULATION LEADS received FDA 510(k) clearance under submission number K051773, sponsored by Medtronic Inc.,Neurological Division.. The device was reviewed via the Special premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2005-07-28.
- Submission: K051773
- Applicant / Sponsor: Medtronic Inc.,Neurological Division.
- Clearance pathway: Special
- Review panel: Neurology
- Device class: Class II
- Regulation citation: 21 CFR 882.5880
- Decision date: 2005-07-28
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.