# K241942: TriMed Bridge Plates

- Pathway: 510(k) (Traditional)
- Applicant: TriMed, Inc.
- Decided: Sep 17, 2024 after 77 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: 5 generations back to K981372 (1998). 13 ancestors in all.
No later device cites it as a predicate yet.
0 of 14 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K131764: Acumed Wrist Spanning Plate, Acumed, LLC (2013) Summary page 5.

## Indications for use
TriMed Bridge Plate is indicated for fixation of fractures, osteotomies, and nonunions of the radius.

Source page: https://510kreport.com/device/K241942
Methodology: https://510kreport.com/methodology