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NC Quantum Apex PTCA Dilatation Catheter

K160823 Class II Special
Decision Date
2016-06-23
Sponsor / Applicant
Boston Scientific Corporation

Technical Specification

510(k) Submission ID K160823
Product Code LOX
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.5100
Decision Date 2016-06-23
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NC Quantum Apex PTCA Dilatation Catheter received FDA 510(k) clearance under submission number K160823, 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 2016-06-23.

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.