# K102785: Trimed Radiocarpal Fusion System

- Pathway: 510(k) (Traditional)
- Applicant: TriMed, Inc.
- Decided: Aug 19, 2011 after 326 days
- Product code: HRS (Plate, Fixation, Bone)
- Device class: 2
- Regulation: 21 CFR 888.3030
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K000684 (2000). 3 ancestors in all.
2 later devices descend from it; 1 cites it directly.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K042355: Synthes (Usa) LCP Wrist Fusion Plates, Synthes (Usa) (2004) Summary page 1.
- K011335: Synths One-Third Tubular DCL Plate, Synthes (Usa) (2001) Summary page 1.

## Most influential descendants
- K251945: TriMed Total Wrist Fusion System (Total Wrist Fusion Plate) (2025), 1 descendant of its own
- K262032: TriMed Non-Spanning Wrist Fusion Plates (NSFL-STD);TriMed Non-Spanning Wrist Fusion Plates (NSFR-STD);TriMed Non-Spanning Wrist Fusion Plates (NSFL-SHB );TriMed Non-Spanning Wrist Fusion Plates (NSFR-SHB ) (2026), 0 descendants of its own

## Indications for use
The TriMed Radiocarpal Fusion System plates and screws are intended for wrist arthrodesis and fixation of fractures of other small bones

Source page: https://510kreport.com/device/K102785
Methodology: https://510kreport.com/methodology