# K160409: AOS Anterolateral Proximal Humeral Plate

- Pathway: 510(k) (Special)
- Applicant: Advanced Orthopaedic Solutions, Inc.
- Decided: Mar 15, 2016 after 28 days
- Product code: KTW (Appliance, Fixation, Nail/Blade/Plate Combination, Single Component)
- 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 K011815 (2001). 2 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K080590: Aos Proximal Humeral Plate, Advanced Orthopaedic Solutions, Inc. (2008) Summary page 4.

## Most influential descendants
- K171606: AOS Anterolateral Proximal Humeral Plate (2017), 0 descendants of its own

## Indications for use
The AOS Anterolateral Proximal Humeral Plate is indicated for fractures, fracture dislocations, osteotomies, and non-unions of the proximal humerus.

Source page: https://510kreport.com/device/K160409
Methodology: https://510kreport.com/methodology