# K203761: ParaMotion

- Pathway: 510(k) (Traditional)
- Applicant: Powerbasetec GmbH
- Decided: Jan 21, 2022 after 394 days
- Product code: IPL (Wheelchair, Standup)
- Device class: 2
- Regulation: 21 CFR 890.3900
- 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 K963817 (1997). 4 ancestors in all.
No later device cites it as a predicate yet.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K060936: Paragolfer, Parabasetec, GmbH (2006) Summary page 5.

## Indications for use
Any individual who needs a power wheelchair and can not stand up on their own such as people with paraplegia, spina bifida, cerebral paresis, multiple sclerosis, muscular dystrophy and polio any individual to take part in sports activities requiring an upright position

Source page: https://510kreport.com/device/K203761
Methodology: https://510kreport.com/methodology