# K233877: XT Series Power Wheelchair  (XT2), XT Series Power Wheelchair  (XT4)

- Pathway: 510(k) (Traditional)
- Applicant: Magic Mobility
- Decided: Mar 4, 2024 after 88 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: 6 generations back to K960951 (1997). 14 ancestors in all.
No later device cites it as a predicate yet.
0 of 15 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K211574: Extreme X8, Magic Mobility (2021) Summary page 6.
- K172384: Quickie (r) Q700-UP M, Sunrise Medical (Us), LLC (2018) Summary page 6.

## Indications for use
The XT2 power wheelchair is a battery-operated device with wheels that is intended for medical purposes to provide mobility to persons restricted to a sitting position who have the capability of operating a power wheelchair. The XT4 power wheelchair is a battery-operated device with wheels that is intended for medical purposes to provide mobility to persons restricted to a sitting position who have the capability of operating a power wheelchair.

Source page: https://510kreport.com/device/K233877
Methodology: https://510kreport.com/methodology