meddevicedb.com FDA Device Reference

NEUROPORT NEURAL SIGNAL PROCESSING SYSTEM

K060523 Class II Special
Decision Date
2006-03-28
Sponsor / Applicant
Cyberkinetics, Inc.

Technical Specification

510(k) Submission ID K060523
Product Code OMC
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.1400
Decision Date 2006-03-28
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NEUROPORT NEURAL SIGNAL PROCESSING SYSTEM received FDA 510(k) clearance under submission number K060523, sponsored by Cyberkinetics, 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 2006-03-28.

Classification & Regulation

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