# K123875: Aap Radius Set 2.5

- Pathway: 510(k) (Traditional)
- Applicant: Aap Implantate AG
- Decided: Mar 11, 2013 after 84 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: 1 generation back to K012114 (2001). 1 ancestor in all.
21 later devices descend from it; 1 cites it directly.
0 of 23 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K012114: Synthes Locking Distal Radius Plating System, Synthes (Usa) (2001) Summary page 1.

## Most influential descendants
- K131474: Arthrex Distal Radius Plate System (2013), 20 descendants of its own
- K201132: Arthrex Compression Screws (2020), 11 descendants of its own
- K150456: Arthrex Plates, Screws, and Staples (2015), 6 descendants of its own
- K143749: Arthrex Distal Radius System (2015), 2 descendants of its own
- K254215: Arthrex Beaming System (2026), 1 descendant of its own

## Indications for use
The aap Radius Set 2.5 is indicated for the fixation of intra- and extra-articular fractures and osteotomies of the distal radius.

Source page: https://510kreport.com/device/K123875
Methodology: https://510kreport.com/methodology