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CTLOGICS NAVIGATIONS SYSTEMS

K063408 Class II Traditional
Decision Date
2007-02-28
Sponsor / Applicant
Praxim Medivision, SA

Technical Specification

510(k) Submission ID K063408
Product Code HAW
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.4560
Decision Date 2007-02-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CTLOGICS NAVIGATIONS SYSTEMS received FDA 510(k) clearance under submission number K063408, sponsored by Praxim Medivision, SA. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2007-02-28.

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.