# K072343: Neurovision JJB System

- Pathway: 510(k) (Traditional)
- Applicant: Nuvasive, Inc.
- Decided: Oct 29, 2007 after 69 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: 4 generations back to K842956 (1984). 10 ancestors in all.
No later device cites it as a predicate yet.
0 of 11 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K062765: Modification to Nuvasive Neurovision JJB System, Nuvasive, Inc. (2007) Summary page 1.
- K051357: DS7A Constant Current High Voltage Stimulator, Model DS7A; DS7AH Constant Current High Voltage Stimulator, Model DS7AH, Digitimer, Ltd. (2005) Summary page 1.
- K032741: Epochxp Neurological Workstation,Epochxp Lite Neurological Workstation, Axon Systems, Inc. (2003) Summary page 2.

## Indications for use
The NeuroVision System is intended for use in the operating room and non-critical care clinical environment for neurological monitoring and status assessment. The System may be used alone or in conjunction with other NuVasive devices to assist in gaining controlled access to the spine.

Source page: https://510kreport.com/device/K072343
Methodology: https://510kreport.com/methodology