meddevicedb.com FDA Device Reference

PERIPHERAL CUTTING BALLOON SMALL MONORAIL OR OVER-THE-WIRE DELIVERY SYSTEM

K052038 Class II Special
Decision Date
2005-08-16
Sponsor / Applicant
Boston Scientific Corporation

Technical Specification

510(k) Submission ID K052038
Product Code LIT
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1250
Decision Date 2005-08-16
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PERIPHERAL CUTTING BALLOON SMALL MONORAIL OR OVER-THE-WIRE DELIVERY SYSTEM received FDA 510(k) clearance under submission number K052038, sponsored by Boston Scientific Corporation. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2005-08-16.

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.