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NC Gallant PTCA Catheter

K162434 Class II Traditional
Decision Date
2017-01-19
Sponsor / Applicant
Medinol, Ltd.

Technical Specification

510(k) Submission ID K162434
Product Code LOX
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.5100
Decision Date 2017-01-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NC Gallant PTCA Catheter received FDA 510(k) clearance under submission number K162434, sponsored by Medinol, Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2017-01-19.

Classification & Regulation

This clearance is catalogued under FDA product code LOX and 21 CFR 870.5100, within the Cardiovascular review panel as a Class II device.