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NAVIGUS II TRAJECTORY GUIDE WITH VERIFICATION RETICULES

K023949 Class II Traditional
Decision Date
2003-02-25
Sponsor / Applicant
Image-Guided Neurologics, Inc.

Technical Specification

510(k) Submission ID K023949
Product Code HAW
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.4560
Decision Date 2003-02-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NAVIGUS II TRAJECTORY GUIDE WITH VERIFICATION RETICULES received FDA 510(k) clearance under submission number K023949, sponsored by Image-Guided Neurologics, 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 2003-02-25.

Classification & Regulation

This clearance is catalogued under FDA product code HAW and 21 CFR 882.4560, within the Neurology review panel as a Class II device.