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NAVAJO PTA BALLOON DILATATION CATHETER

K141354 Class II Traditional
Decision Date
2015-01-30
Sponsor / Applicant
Curative Medical, Inc.

Technical Specification

510(k) Submission ID K141354
Product Code DQY
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1250
Decision Date 2015-01-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NAVAJO PTA BALLOON DILATATION CATHETER received FDA 510(k) clearance under submission number K141354, sponsored by Curative Medical, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2015-01-30.

Classification & Regulation

This clearance is catalogued under FDA product code DQY and 21 CFR 870.1250, within the Cardiovascular review panel as a Class II device.