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COMPONENT NEUROMONITORING SYSTEM

K080217 Class II Traditional
Decision Date
2008-11-05
Sponsor / Applicant
Moberg Research, Inc.

Technical Specification

510(k) Submission ID K080217
Product Code OMA
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.1400
Decision Date 2008-11-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

COMPONENT NEUROMONITORING SYSTEM received FDA 510(k) clearance under submission number K080217, sponsored by Moberg Research, 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 2008-11-05.

Classification & Regulation

This clearance is catalogued under FDA product code OMA and 21 CFR 882.1400, within the Neurology review panel as a Class II device.