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GLADIATOR ELITE PTA BALLOON DILATATION CATHETER

K132810 Class II Traditional
Decision Date
2014-02-28
Sponsor / Applicant
Boston Scientific Corp

Technical Specification

510(k) Submission ID K132810
Product Code LIT
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1250
Decision Date 2014-02-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

GLADIATOR ELITE PTA BALLOON DILATATION CATHETER received FDA 510(k) clearance under submission number K132810, sponsored by Boston Scientific Corp. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2014-02-28.

Classification & Regulation

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