# K171606: AOS Anterolateral Proximal Humeral Plate

- Pathway: 510(k) (Special)
- Applicant: Advanced Orthopaedic Solutions, Inc. (Aos)
- Decided: Jun 22, 2017 after 21 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: 3 generations back to K011815 (2001). 4 ancestors in all.
No later device cites it as a predicate yet.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K160409: AOS Anterolateral Proximal Humeral Plate, Advanced Orthopaedic Solutions, Inc. (2016) Summary page 4.
- K041860: Synthes (Usa) LCP Proximal Humerus Plates, Long, Synthes (Usa) (2004) Summary page 4.

## 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/K171606
Methodology: https://510kreport.com/methodology