# K201869: Ki Power Tilt System

- Pathway: 510(k) (Traditional)
- Applicant: Ki Mobility, LLC
- Decided: Sep 5, 2023 after 1,155 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 K972564 (1997). 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)
- K972564: Tilt Master CG System (Center of Gravity), Tilt-N-Space-Seat, Mechanical Application Designs, Inc. (1997) Summary page 4.

## Indications for use
The Ki Mobility Power Tilt System kit design is intended for use on a manual wheelchair to provide patients with posterior tilt for positioning and seating pressure relief.

Source page: https://510kreport.com/device/K201869
Methodology: https://510kreport.com/methodology