meddevicedb.com FDA Device Reference

NUVASIVE NEUROVISION JJB SYSTEM

K051718 Class II Traditional
Decision Date
2005-09-15
Sponsor / Applicant
Nuvasive, Inc.

Technical Specification

510(k) Submission ID K051718
Product Code ETN
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.1820
Decision Date 2005-09-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NUVASIVE NEUROVISION JJB SYSTEM received FDA 510(k) clearance under submission number K051718, sponsored by Nuvasive, 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 2005-09-15.

Classification & Regulation

This clearance is catalogued under FDA product code ETN and 21 CFR 874.1820, within the Ear, Nose, Throat review panel as a Class II device.