# K890076: Orthotrak

- Pathway: 510(k) (Traditional)
- Applicant: Motion Analysis Corp.
- Decided: Feb 3, 1989 after 25 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
No predicates in its family tree.
14 later devices descend from it; 1 cites it directly.
0 of 15 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K982425: Coda MPX30 Motion Analysis System (1998), 13 descendants of its own
- K033514: Coda CX1 Motion Analysis System (2004), 10 descendants of its own
- K030714: Peak Motus (2003), 10 descendants of its own
- K130847: Jintronix Rehabilitation System (JRS) (2014), 6 descendants of its own
- K151446: Recovr Rehabilitation System (2015), 1 descendant of its own

Source page: https://510kreport.com/device/K890076
Methodology: https://510kreport.com/methodology