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RADIONICS RF DISC CATHETER ELECTRODE SYSTEM

K001741 Class II Traditional
Decision Date
2000-10-23
Sponsor / Applicant
Radionics, Inc.

Technical Specification

510(k) Submission ID K001741
Product Code HRX
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.1100
Decision Date 2000-10-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

RADIONICS RF DISC CATHETER ELECTRODE SYSTEM received FDA 510(k) clearance under submission number K001741, sponsored by Radionics, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2000-10-23.

Classification & Regulation

This clearance is catalogued under FDA product code HRX and 21 CFR 888.1100, within the Orthopedic review panel as a Class II device.