# K051718: Nuvasive Neurovision JJB System

- Pathway: 510(k) (Traditional)
- Applicant: Nuvasive, Inc.
- Decided: Sep 15, 2005 after 80 days
- Product code: ETN (Stimulator, Nerve)
- Device class: 2
- Regulation: 21 CFR 874.1820
- 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 no predicate by number.

## Most influential descendants
- K111671: Seaspine Monopolar Probe Sysyem (2011), 0 descendants of its own

## Indications for use
The NeuroVision JJB System is used for intraoperative monitoring and neurological status assessment by the administration of brief electrical stimulus pulses to neural tissues and the EMG monitoring of the associated muscle groups. The System is used in conjunction with other NuVasive devices to assist in gaining controlled access to, and visualization of, the spine.

Source page: https://510kreport.com/device/K051718
Methodology: https://510kreport.com/methodology