# K213090: Frontier Series Power Wheelchairs

- Pathway: 510(k) (Traditional)
- Applicant: Magic Mobility
- Decided: Nov 19, 2021 after 56 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 K900565 (1990). 9 ancestors in all.
No later device cites it as a predicate yet.
0 of 10 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K030783: Frontier Model X5, Vestil Manufacturing Corp. (2003) Summary page 4.
- K142457: Quickie, Zippie, Sunrise Medical (Us), LLC (2014) Summary page 4.

## Indications for use
The Frontier Series Power Wheelchairs are battery-operated devices with wheels that are 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/K213090
Methodology: https://510kreport.com/methodology