# K170537: Nexxis OR, Nexxis

- Pathway: 510(k) (Special)
- Applicant: Barco N.V.
- Decided: Apr 21, 2017 after 57 days
- Product code: DXJ (Display, Cathode-Ray Tube, Medical)
- Device class: 2
- Regulation: 21 CFR 870.2450
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K122167 (2013). 2 ancestors in all.
2 later devices descend from it; 1 cites it directly.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K133994: SIVR56-T Kit, Barco N.V. (2014) Summary page 4.
- K122167: Nexxis or, Barco N.V. (2013) Summary page 4.

## Most influential descendants
- K173381: Nexxis OR (2018), 1 descendant of its own
- K261469: Nexxis 2;Nexxis OR 2;NMS 2;MNA-240;MNA-4x0 (Where “x” may be any numeric character). (2026), 0 descendants of its own

## Indications for use
The Barco Nexxis OR system is designed to allow transfer, selection and distribution of A/V signals and medical images from various commercially available instruments that are commonly used in a medical procedure laboratory or operating room. The Barco Nexxis OR system is also designed for transfer, selection and distribution of human interface signals and control signals of non-medical room equipment, The Barco Nexxis OR system allows control and selection of these signals from a central point. The Barco Nexxis OR system is not intended to be used for remote or robotically assisted surgery, The Barco Nexxis OR system is not intended to be used in the vicinity of MRI or other devices that use strong magnetic fields.

Source page: https://510kreport.com/device/K170537
Methodology: https://510kreport.com/methodology