# KWG: Prosthesis, Finger, Constrained, Metal/Polymer

- Device class: 3; regulation: 21 CFR 888.3220; FDA's rule: PMA 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)
- 1997: 1
- 1998: 2
- 2002: 1
- 2007: 1
- 2016: 1

## Most-cited predicates

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