# JDP: Condylar Plate Fixation Implant

- Device class: 2; regulation: 21 CFR 888.3030; FDA's rule: 510(k) required
- FDA decisions: 2
- Recalls: 1 (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)
- 2011: 1
- 2017: 1

## Most-cited predicates
- K110354: 4.5MM VA-LCP Curved Condylar Plate System (2011), cited by 6
- K162124: Synthes 4.5mm VA-LCP Curved Condylar Plate System Line Extension, Variable Angle Positioning Pins (2017), cited by 4

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