Clearance Summary
KARL STORZ NAV1 Electromagnetic Navigation System received FDA 510(k) clearance under submission number K161555, sponsored by Karl Storz Endoscopy America, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2016-10-21.
- Submission: K161555
- Applicant / Sponsor: Karl Storz Endoscopy America, Inc.
- Clearance pathway: Traditional
- Review panel: Neurology
- Device class: Class II
- Regulation citation: 21 CFR 882.4560
- Decision date: 2016-10-21
Classification & Regulation
This clearance is catalogued under FDA product code PGW and 21 CFR 882.4560, within the Neurology review panel as a Class II device.