# NDK: System, External Fixator (With Metallic Invasive Components)

- Device class: 2; regulation: 21 CFR 888.3040; FDA's rule: 510(k) required
- FDA decisions: 3
- 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)
- 2010: 1
- 2012: 1
- 2014: 1

## Most-cited predicates
- K101375: Trimed X-Fix (2010), cited by 1

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