# GAK: Suture, Absorbable

- Device class: 2; regulation: 21 CFR 878.4830; FDA's rule: 510(k) required
- FDA decisions: 1
- 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)
- 1980: 6
- 1981: 10
- 1982: 3
- 1984: 4
- 1986: 2
- 1987: 1
- 1991: 1

## Most-cited predicates

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