# K131094: Vimove

- Pathway: 510(k) (Traditional)
- Applicant: Dorsa VI Pty., Ltd.
- Decided: Jul 11, 2014 after 449 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: 4 generations back to K971407 (1998). 7 ancestors in all.
No later device cites it as a predicate yet.
0 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K063447: Insight Discovery, Fasstech (2007) Summary page 2.
- K811172: VICON, Oxford Medilog, Inc. (1981) Summary page 1.

## Indications for use
ViMove 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/K131094
Methodology: https://510kreport.com/methodology