# K163150: ViMove2

- Pathway: 510(k) (Special)
- Applicant: Dorsavi, Ltd.
- Decided: Jul 14, 2017 after 247 days
- Product code: IKN (Electromyograph, Diagnostic)
- Device class: 2
- Regulation: 21 CFR 890.1375
- 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 K142494 (2015). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K142494: ViMove, Dorsavi, Ltd. (2015) Summary page 5.

## Indications for use
ViMove2 is a wireless medical device that measures, records, and reports movements and muscle activity of the lower back / lumbar spine. The system also measures range of motion in the sagittal and coronal anatomical planes.

Source page: https://510kreport.com/device/K163150
Methodology: https://510kreport.com/methodology