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NEUROSENSOR CEREBRAL BLOOD FLOW AND INTRACRANIAL PRESSURE MONITORING KIT/SYSTEM, MODELS NS-P, NS-100

K050720 Class II Special
Decision Date
2005-05-11
Sponsor / Applicant
Integra Neurosciences

Technical Specification

510(k) Submission ID K050720
Product Code GWM
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.1620
Decision Date 2005-05-11
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NEUROSENSOR CEREBRAL BLOOD FLOW AND INTRACRANIAL PRESSURE MONITORING KIT/SYSTEM, MODELS NS-P, NS-100 received FDA 510(k) clearance under submission number K050720, sponsored by Integra Neurosciences. The device was reviewed via the Special premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2005-05-11.

Classification & Regulation

This clearance is catalogued under FDA product code GWM and 21 CFR 882.1620, within the Neurology review panel as a Class II device.