# K024279: Ness Children System

- Pathway: 510(k) (Traditional)
- Applicant: Ness-Neuromuscular Electrical Stimulation Systems
- Decided: Feb 5, 2003 after 44 days
- Product code: IPG (Shoe, Cast)
- Device class: 1
- Regulation: 21 CFR 890.3025
- 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 K813008 (1981). 6 ancestors in all.
No later device cites it as a predicate yet.
0 of 7 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K022776: Ness System, Ness-Neuromuscular Electrical Stimulation Systems (2002)

## Indications for use
The NESS Children System is intended for pediatric use for the following indications: maintenance or increase of range of motion, reduction of muscle spasm, prevention or retardation of disuse atrophy, muscle reeducation, and increasing local blood circulation.

Source page: https://510kreport.com/device/K024279
Methodology: https://510kreport.com/methodology