# K033514: Coda CX1 Motion Analysis System

- Pathway: 510(k) (Traditional)
- Applicant: Charnwood Dynamics, Ltd.
- Decided: Jan 6, 2004 after 61 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; 3 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
- K171547: Qualisys Clinical System (2018), 0 descendants of its own
- K172882: Uincare Home (2018), 0 descendants of its own

## Indications for use
The Coda cx I Motion Analysis System has general application to measurement and recording of 3D position and movement, including human movement. It is appropriate for use in assessment of the 3D motion of the limbs and body of patients who have some impairment of movement functions of either a neurological or orthopaedic cause.

Source page: https://510kreport.com/device/K033514
Methodology: https://510kreport.com/methodology