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NAVIGATION SW HIP 3.1 ON CI

K052213 Class II Special
Decision Date
2005-11-02
Sponsor / Applicant
Brainlab AG

Technical Specification

510(k) Submission ID K052213
Product Code HAW
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.4560
Decision Date 2005-11-02
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NAVIGATION SW HIP 3.1 ON CI received FDA 510(k) clearance under submission number K052213, sponsored by Brainlab AG. The device was reviewed via the Special premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2005-11-02.

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.