meddevicedb.com FDA Device Reference

NC QUANTUM APEX PTCA DILATATION CATHETER (MONORAIL)

K121667 Class II Special
Decision Date
2012-08-13
Sponsor / Applicant
Boston Scientific Corp

Technical Specification

510(k) Submission ID K121667
Product Code LOX
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.5100
Decision Date 2012-08-13
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NC QUANTUM APEX PTCA DILATATION CATHETER (MONORAIL) received FDA 510(k) clearance under submission number K121667, sponsored by Boston Scientific Corp. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2012-08-13.

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.