# K031289: Quickie Freestyle Power Wheelchair, Model G-424

- Pathway: 510(k) (Special)
- Applicant: Sunrise Medical, Inc.
- Decided: May 9, 2003 after 16 days
- Product code: ITI (Wheelchair, Powered)
- Device class: 2
- Regulation: 21 CFR 890.3860
- Recalls of this device: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
10 later devices descend from it; 1 cites it directly.
0 of 11 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K051387: Levo Comfort II (2005), 9 descendants of its own
- K083017: LEVO C3 (2008), 4 descendants of its own
- K172384: Quickie (r) Q700-UP M (2018), 2 descendants of its own
- K060936: Paragolfer (2006), 1 descendant of its own
- K233877: XT Series Power Wheelchair  (XT2), XT Series Power Wheelchair  (XT4) (2024), 0 descendants of its own

## Recalls of this device
- Nov 15, 2005 · Not classified · Z-0518-06: While operating the powered wheelchair beyond a specified angle of recline, the wheelchair can travel at an unsafe speed when in this position.

## Indications for use
The Center Drive Power Wheelchair’s intended use is to empower physically challenged individuals by providing a means of mobility.

Source page: https://510kreport.com/device/K031289
Methodology: https://510kreport.com/methodology