# K024055: Tilite Evo

- Pathway: 510(k) (Traditional)
- Applicant: Tisport, LLC
- Decided: Dec 20, 2002 after 11 days
- Product code: IOR (Wheelchair, Mechanical)
- Device class: 1
- Regulation: 21 CFR 890.3850
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K925451 (1993). 2 ancestors in all.
No later device cites it as a predicate yet.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K990358: Cross Sport, Rigid Wheelchair, Tisport (1999) Summary page 2.

## Indications for use
The intended use of this device (manual, rigid wheelchair) is the same as the predicate device, the TiSport Cross-Sport (manual, rigid wheelchair) manufactured by TiSport, LLC. The intended use for the manual, rigid wheelchair is to provide mobility to physically persons. The manual wheelchair is intended for ongoing daily use This device is indicated for individuals with the specific medical conditions listed, but the indications are not necessarily limited to such conditions: - Amputee; - Arthritis; - Arthrogriposis; - Cerebral Palsy; - Geriatric conditions; - Head injury or trauma; - Hemiplegic; - Multiple Sclerosis; - Muscular Dystrophy; - Paraplegic; - Polio; - Quadraplegic; - Spina Bifida; - StokeKVA; - Tetraplegic; and - Other immobilizing or debilitating conditions, including spinal cord injuries and other lower and upper extremity paralysis

Source page: https://510kreport.com/device/K024055
Methodology: https://510kreport.com/methodology