# K151825: Viradius Neurowire

- Pathway: 510(k) (Traditional)
- Applicant: Mivi Neuroscience, Inc.
- Decided: Nov 16, 2015 after 133 days
- Product code: MOF (Guide, Wire, Catheter, Neurovasculature)
- Device class: 2
- Regulation: 21 CFR 870.1330
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K991646 (1999). 4 ancestors in all.
No later device cites it as a predicate yet.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K100351: Neuroscout Steerable Guidewire, Codman & Shurtleff, Inc. (2010) Summary page 4.

## Indications for use
The Viradius™ Neurowire is intended for selective placement of catheters within the neuro and peripheral vasculature.

Source page: https://510kreport.com/device/K151825
Methodology: https://510kreport.com/methodology