# K262975: Arthrex Beaming System

- Pathway: 510(k) (Special)
- Applicant: Arthrex, Inc.
- Decided: Sep 25, 2026 after 30 days
- Product code: HWC (Screw, Fixation, Bone)
- Device class: 2
- Regulation: 21 CFR 888.3040
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 14 generations back to K000684 (2000). 96 ancestors in all.
No later device cites it as a predicate yet.
0 of 97 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K254215: Arthrex Beaming System, Arthrex, Inc. (2026) Summary page 5.

## Indications for use
The Arthrex Beaming System is intended to be used in the stabilization, reconstruction, and fixation of bone fractures, fusions, osteotomies, and non-unions in the foot and ankle.

Source page: https://510kreport.com/device/K262975
Methodology: https://510kreport.com/methodology