# K072371: Odyssey Workstation

- Pathway: 510(k) (Traditional)
- Applicant: Stereotaxis, Inc.
- Decided: Nov 14, 2007 after 83 days
- Product code: DXX (System, Catheter Control, Steerable)
- Device class: 2
- Regulation: 21 CFR 870.1290
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Stereotaxis, Niobe MNS w/Navigant NWS: named in the summary without a submission number
- (no number) Navigant Workstation w/Niobe Magnetic Navigation System, Version NWS05: named in the summary without a submission number
- (no number) Navigant Navigation Workstation 2.1: named in the summary without a submission number
- (no number) Stereotaxis Niobe Magnetic Navigation System: named in the summary without a submission number

## Most influential descendants
- K253473: Synchrony (2026), 0 descendants of its own

## Indications for use
The Odyssey Workstation is: an optional display and user interface package designed to consolidate the point of control in the Catheter Lab.

Source page: https://510kreport.com/device/K072371
Methodology: https://510kreport.com/methodology