Clearance Summary
MEDTRONIC PS MEDICAL INNERVISION VENTRICULAR CATHETER, 15CM MODEL 99102 received FDA 510(k) clearance under submission number K983331, sponsored by Medtronic PS Medical. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 1998-12-16.
- Submission: K983331
- Applicant / Sponsor: Medtronic PS Medical
- Clearance pathway: Traditional
- Review panel: Neurology
- Device class: Class II
- Regulation citation: 21 CFR 882.4100
- Decision date: 1998-12-16
Classification & Regulation
This clearance is catalogued under FDA product code HCA and 21 CFR 882.4100, within the Neurology review panel as a Class II device.