meddevicedb.com FDA Device Reference

Pantheris System

K152275 Class II Traditional
Decision Date
2015-10-14
Sponsor / Applicant
Avinger, Inc.

Technical Specification

510(k) Submission ID K152275
Product Code MCW
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.4875
Decision Date 2015-10-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Pantheris System received FDA 510(k) clearance under submission number K152275, sponsored by Avinger, 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 2015-10-14.

Classification & Regulation

This clearance is catalogued under FDA product code MCW and 21 CFR 870.4875, within the Cardiovascular review panel as a Class II device.