# K143034: Jintronix

- Pathway: 510(k) (Traditional)
- Applicant: Jintronix, Inc.
- Decided: Apr 22, 2015 after 182 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 5.
- K030714: Peak Motus, Peak Performance Technologies, Inc. (2003) Summary page 5.

## Indications for use
Jintronix is a software system used with the Microsoft Kinect v2 intended to be used to support the physical rehabilitation of adults in the clinic/ at home. The system includes rehabilitation exercises for the upper extremity, trunk, and lower extremity with audio-visual feedback & graphic movement representations for patients as well as remotely accessible 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/K143034
Methodology: https://510kreport.com/methodology