# K163245: Virtual Occupational Therapy Application (VOTA)

- Pathway: 510(k) (Traditional)
- Applicant: Barron Associates, Inc.
- Decided: Feb 28, 2017 after 102 days
- Product code: LXJ (Interactive Rehabilitation Exercise Devices)
- Device class: 2
- Regulation: 21 CFR 890.5360
- 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 K890076 (1989). 5 ancestors in all.
No later device cites it as a predicate yet.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K130847: Jintronix Rehabilitation System (JRS), Jintronix, Inc. (2014) Summary page 4.

## Indications for use
A software system used with the Microsoft Kinect intended to be used to support repetitive task practice for rehabilitation of adults under supervision of a medical professional in a clinical or home setting. The system includes simulated activities of daily living (ADLs) for the upper extremity with audio-visual feedback & graphic movement representations for patients as well as patient performance metrics for the medical professional. Patient assessment, exercise guidance, and approval by the medical professional is required prior to use.

Source page: https://510kreport.com/device/K163245
Methodology: https://510kreport.com/methodology