# QTD: Endoscopic Suturing Device For Altering Gastric Anatomy For Weight Loss

- Device class: 2; regulation: 21 CFR 876.5983; FDA's rule: 510(k) required
- FDA decisions: 2
- 510(k) review time 2021–2025: median 27 days (middle half 27–27)
- 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: 1
- 2023: 1

## Most-cited predicates
- DEN210045: APOLLO ESG System, APOLLO ESG SX System, APOLLO REVISE System, APOLLO REVISE SX System (2022), cited by 1

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