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NIOBE MAGNETIC NAVIGATION SYSTEM W/NAVIGANT WORKSTATION

K060967 Class II Traditional
Decision Date
2006-10-19
Sponsor / Applicant
Stereotaxis, Inc.

Technical Specification

510(k) Submission ID K060967
Product Code NDQ
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1290
Decision Date 2006-10-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NIOBE MAGNETIC NAVIGATION SYSTEM W/NAVIGANT WORKSTATION received FDA 510(k) clearance under submission number K060967, sponsored by Stereotaxis, 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 2006-10-19.

Classification & Regulation

This clearance is catalogued under FDA product code NDQ and 21 CFR 870.1290, within the Cardiovascular review panel as a Class II device.