# K240105: Navigator (FMNVG15); Navigator XL (FMNVX06)

- Pathway: 510(k) (Traditional)
- Applicant: Forcemech International, LLC
- Decided: Aug 29, 2024 after 226 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: 5 generations back to K023148 (2003). 5 ancestors in all.
2 later devices descend from it; 1 cites it directly.
0 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K232193: Electrically Power Wheelchairs (Models:YLB-W-0812-A01, YLB-W-0812-A02, YLB-W-0812-A03), Yurob Rehabilitation Medical Co., Ltd. (2023) Summary page 5.

## Most influential descendants
- K244003: Electrically powered wheelchair (2025), 1 descendant of its own
- K251159: Power wheelchair (2025), 0 descendants of its own

## Indications for use
The Navigator (model: FMNVG15) and Navigator XL (model: FMNVX06) is a motor driven, indoor and outdoor transportation vehicle with the intended use to provide mobility to a disabled or elderly person limited to a seated position.

Source page: https://510kreport.com/device/K240105
Methodology: https://510kreport.com/methodology