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HELIX SHAPED COILS WITH DACRON FIBERS, MODIFIED

K911779 Class II Traditional
Decision Date
1991-11-08
Sponsor / Applicant
Target Therapeutics

Technical Specification

510(k) Submission ID K911779
Product Code HCG
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.5950
Decision Date 1991-11-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HELIX SHAPED COILS WITH DACRON FIBERS, MODIFIED received FDA 510(k) clearance under submission number K911779, sponsored by Target Therapeutics. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 1991-11-08.

Classification & Regulation

This clearance is catalogued under FDA product code HCG and 21 CFR 882.5950, within the Neurology review panel as a Class II device.