meddevicedb.com FDA Device Reference

NAVIGUS UNIBODY FIDUCIAL MARKER SYSTEM, MODEL FM-4000

K033619 Class II Traditional
Decision Date
2004-03-02
Sponsor / Applicant
Image-Guided Neurologics, Inc.

Technical Specification

510(k) Submission ID K033619
Product Code HAW
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.4560
Decision Date 2004-03-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NAVIGUS UNIBODY FIDUCIAL MARKER SYSTEM, MODEL FM-4000 received FDA 510(k) clearance under submission number K033619, 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 2004-03-02.

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.