meddevicedb.com FDA Device Reference

RADIONICS CONTOUR FLEX VALVE, RADIONICS CONTOUR FLEX PLUS VALVE

K971511 Class II Traditional
Decision Date
1997-07-24
Sponsor / Applicant
Radionics, Inc.

Technical Specification

510(k) Submission ID K971511
Product Code JXG
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.5550
Decision Date 1997-07-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

RADIONICS CONTOUR FLEX VALVE, RADIONICS CONTOUR FLEX PLUS VALVE received FDA 510(k) clearance under submission number K971511, sponsored by Radionics, 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 1997-07-24.

Classification & Regulation

This clearance is catalogued under FDA product code JXG and 21 CFR 882.5550, within the Neurology review panel as a Class II device.