meddevicedb.com FDA Device Reference

iCE-SG Subcutaneous Electrode Arrays

K201678 Class II Traditional
Decision Date
2021-03-08
Sponsor / Applicant
Ice Neurosystems, Inc.

Technical Specification

510(k) Submission ID K201678
Product Code GZL
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.1330
Decision Date 2021-03-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

iCE-SG Subcutaneous Electrode Arrays received FDA 510(k) clearance under submission number K201678, sponsored by Ice Neurosystems, 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 2021-03-08.

Classification & Regulation

This clearance is catalogued under FDA product code GZL and 21 CFR 882.1330, within the Neurology review panel as a Class II device.