# K030714: Peak Motus

- Pathway: 510(k) (Traditional)
- Applicant: Peak Performance Technologies, Inc.
- Decided: May 16, 2003 after 71 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: 2 generations back to K890076 (1989). 2 ancestors in all.
10 later devices descend from it; 4 cite it directly.
0 of 13 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K982425: Coda MPX30 Motion Analysis System, Pinsco Inc. Dba B & L Engineering (1998) Summary page 1.

## Most influential descendants
- K130847: Jintronix Rehabilitation System (JRS) (2014), 6 descendants of its own
- K151446: Recovr Rehabilitation System (2015), 1 descendant of its own
- K131660: Smart (Smart-D, Smart-DX) (2014), 1 descendant of its own
- K180880: DARI Health (2019), 0 descendants of its own
- K171547: Qualisys Clinical System (2018), 0 descendants of its own

## Indications for use
Computer and video system used to quantify and graphically display human movement patterns and techniques for uses such as assessment and training of limb or body motion in gait analysis, prosthetic design, pre/post rehabilitation evaluation, physical therapy, and the like.

Source page: https://510kreport.com/device/K030714
Methodology: https://510kreport.com/methodology