# K242430: Power-Flex (PFX1214); Power-Flex (PFX1517); Power-Flex (PFX1820)

- Pathway: 510(k) (Traditional)
- Applicant: Soul Mobility
- Decided: Nov 12, 2024 after 89 days
- Product code: ITI (Wheelchair, Powered)
- Device class: 2
- Regulation: 21 CFR 890.3860
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K231032 (2023). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K231032: AMP by Method Mobility, AMP Plus (or +) by Method Mobility, Method Mobility (2023) Summary page 6.

## Indications for use
The Power-Flex by Soul Mobility is intended to provide enhanced mobility to disabled persons who are capable of operating a powered and manual wheelchair, by providing powered mobility to manual wheelchairs.

Source page: https://510kreport.com/device/K242430
Methodology: https://510kreport.com/methodology