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Element System with IBT Electrodes

K173571 Class II Traditional
Decision Date
2018-03-21
Sponsor / Applicant
Infinite Biomedical Technologies, LLC

Technical Specification

510(k) Submission ID K173571
Product Code GXY
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.1320
Decision Date 2018-03-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Element System with IBT Electrodes received FDA 510(k) clearance under submission number K173571, sponsored by Infinite Biomedical Technologies, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2018-03-21.

Classification & Regulation

This clearance is catalogued under FDA product code GXY and 21 CFR 882.1320, within the Neurology review panel as a Class II device.