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NEUROMATE STEREOTACTIC SYSTEM

K963256 Class II Traditional
Decision Date
1997-05-09
Sponsor / Applicant
Integrated Surgical Systems, S.A.

Technical Specification

510(k) Submission ID K963256
Product Code HAW
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.4560
Decision Date 1997-05-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NEUROMATE STEREOTACTIC SYSTEM received FDA 510(k) clearance under submission number K963256, sponsored by Integrated Surgical Systems, S.A.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 1997-05-09.

Classification & Regulation

This clearance is catalogued under FDA product code HAW and 21 CFR 882.4560, within the Neurology review panel as a Class II device.