# QPT: Stimulator, Tibial, Electrical, Implantable, For Urinary Incontinence

- Device class: 3; regulation: 21 CFR —; FDA's rule: PMA required
- FDA decisions: 2
- Recalls: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026; MAUDE to Sep 30, 2026

## Decisions per year (last 10)
- 2022: 4
- 2023: 2
- 2025: 7
- 2026: 14

## Most-cited predicates

Source page: https://510kreport.com/product-code/QPT
Data by year (CSV): https://510kreport.com/product-code/QPT.csv