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MTS MULTIPROGRAM TRIAL STIMULATOR SYSTEM

K033757 Class II Traditional
Decision Date
2004-01-30
Sponsor / Applicant
Advanced Neuromodulation Systems

Technical Specification

510(k) Submission ID K033757
Product Code GZB
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.5880
Decision Date 2004-01-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MTS MULTIPROGRAM TRIAL STIMULATOR SYSTEM received FDA 510(k) clearance under submission number K033757, sponsored by Advanced Neuromodulation Systems. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2004-01-30.

Classification & Regulation

This clearance is catalogued under FDA product code GZB and 21 CFR 882.5880, within the Neurology review panel as a Class II device.