# K110140: Neurovision Nerve Locator Monitor

- Pathway: 510(k) (Traditional)
- Applicant: Neurovision Medical Products, Inc.
- Decided: Sep 30, 2011 after 255 days
- Product code: GWF (Stimulator, Electrical, Evoked Response)
- Device class: 2
- Regulation: 21 CFR 882.1870
- 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 K954601 (1995). 2 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K954601: Nerve Locator/Monitor System Modification, Rln Systems, Inc. (1995) Summary page 1.
- K002677: Nuvasive Ins-1 Intraoperative Nerve Surveillance System, Nuvasive, Inc. (2000) Summary page 1.

## Most influential descendants
- K121931: Nondisposable Stimulating Instruments (2012), 0 descendants of its own

## Indications for use
The Neurovision Nerve Locator Monitor is an electronic device consisting of a surgical nerve stimulator and an evoked EMG Monitor with integrated detecting or warning capability. The device is intended to assist the surgeon in locating motor nerves that are at risk in surgical procedures.

Source page: https://510kreport.com/device/K110140
Methodology: https://510kreport.com/methodology