# K012909: Xterra GT Power Wheelchair

- Pathway: 510(k) (Traditional)
- Applicant: Invacare Corp.
- Decided: Oct 24, 2001 after 55 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: 3 generations back to K900565 (1990). 4 ancestors in all.
14 later devices descend from it; 3 cite it directly.
0 of 19 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K991168: Arrow FWD Power Wheelchair, Invacare Corp. (1999) Summary page 1.
- K960951: Permobil Chairman L/CS 8, Permobil AB (1997) Summary page 1.

## Most influential descendants
- K023589: Storm TDX Power Wheelchair (2002), 9 descendants of its own
- K141783: TDX SP2 Power Wheechair (2015), 4 descendants of its own
- K170507: Invacare® TDX® SP2 Power Wheelchair; TDXSP2 TDX SP2 with LiNX Electronics, TDXSP2-CG TDX SP2 Base for Single Act. System w/ Ultra Low Maxx, TDXSP2-MCG TDX SP2 Base for Multiple Actuator System w/ Ultra Low Maxx (2017), 3 descendants of its own
- K192216: Invacare AVIVA FX Power Wheelchair, Model: IFX-20MP (2020), 1 descendant of its own
- K092225: Amypower All Track Series Power Wheelchair (2009), 1 descendant of its own

## Indications for use
The intended use of the Invacare ZX2 Power Wheelchair is to provide mobility to persons limited to a sitting position, that have the capability of operating a powered wheelchair.

Source page: https://510kreport.com/device/K012909
Methodology: https://510kreport.com/methodology