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ODYSSEY WORKSTATION

K093092 Class II Special
Decision Date
2010-01-21
Sponsor / Applicant
Stereotaxis, Inc.

Technical Specification

510(k) Submission ID K093092
Product Code DQK
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1425
Decision Date 2010-01-21
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ODYSSEY WORKSTATION received FDA 510(k) clearance under submission number K093092, sponsored by Stereotaxis, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2010-01-21.

Classification & Regulation

This clearance is catalogued under FDA product code DQK and 21 CFR 870.1425, within the Cardiovascular review panel as a Class II device.