# K073432: Trauson Bone Plate

- Pathway: 510(k) (Traditional)
- Applicant: Trauson (Jiangsu) Medical Instrument Co., Ltd.
- Decided: Aug 13, 2008 after 251 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 K983853 (1998). 6 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K041965: Arthrex Humeral Fracture Plates and Screws, Arthrex, Inc. (2004) Summary page 2.

## Most influential descendants
- K142943: Metallic Locking Bone Plate and Screw (2015), 0 descendants of its own

## Indications for use
Trauson Bone Plate is intended for the fixation of fractures of humerus.

Source page: https://510kreport.com/device/K073432
Methodology: https://510kreport.com/methodology