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Voyager Trajectory Array Guide (V-TAG)

K191400 Class II Special
Decision Date
2019-06-21
Sponsor / Applicant
Mri Interventions, Inc.

Technical Specification

510(k) Submission ID K191400
Product Code HAW
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.4560
Decision Date 2019-06-21
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Voyager Trajectory Array Guide (V-TAG) received FDA 510(k) clearance under submission number K191400, sponsored by Mri Interventions, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2019-06-21.

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.