# K062765: Modification to Nuvasive Neurovision JJB System

- Pathway: 510(k) (Special)
- Applicant: Nuvasive, Inc.
- Decided: Jan 24, 2007 after 117 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
No predicates in its family tree.
2 later devices descend from it; 2 cite it directly.
0 of 3 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 its predicate without a number.
- (no number) Neuro Vision JJB System: named in the summary without a submission number

## Most influential descendants
- K110696: Neuro Check Device with IO-Flex Wire (2011), 0 descendants of its own
- K072343: Neurovision JJB System (2007), 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/K062765
Methodology: https://510kreport.com/methodology