meddevicedb.com FDA Device Reference

XPS Nexus System, XPS Nexus Foot Control, XPS Nexus IV Pole

K150728 Class II Traditional
Decision Date
2015-08-14
Sponsor / Applicant
Medtronic Xomed, Inc.

Technical Specification

510(k) Submission ID K150728
Product Code ERL
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.4250
Decision Date 2015-08-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

XPS Nexus System, XPS Nexus Foot Control, XPS Nexus IV Pole received FDA 510(k) clearance under submission number K150728, sponsored by Medtronic Xomed, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ear, Nose, Throat review panel. The statutory decision date of record is 2015-08-14.

Classification & Regulation

This clearance is catalogued under FDA product code ERL and 21 CFR 874.4250, within the Ear, Nose, Throat review panel as a Class II device.