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NEUROPORT CORTICAL MICROELECTRODE ARRAY SYSTEM

K110010 Class II Special
Decision Date
2011-02-09
Sponsor / Applicant
Blackrock Microsystems, Inc.

Technical Specification

510(k) Submission ID K110010
Product Code GZL
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.1330
Decision Date 2011-02-09
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NEUROPORT CORTICAL MICROELECTRODE ARRAY SYSTEM received FDA 510(k) clearance under submission number K110010, sponsored by Blackrock Microsystems, 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 2011-02-09.

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.