# K132787: Loqteq Distal Dorsolateral Humerus Plate

- Pathway: 510(k) (Traditional)
- Applicant: Aap Implantate AG
- Decided: Dec 24, 2013 after 109 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 K033995 (2004). 1 ancestor in all.
1 later device descends from it; 1 cites it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K033995: 3.5 MM LCP Distal Humerus System, Synthes (Usa) (2004) Summary page 4.

## Most influential descendants
- K230141: LOQTEQ® VA Elbow Plates 2.7/3.5 System (2023), 0 descendants of its own

## Indications for use
The aap LOQTEQ® Elbow System is indicated for: x intra-articular fractures of the distal Humerus x supracondylar fractures of the distal Humerus x osteotomies, and non-unions of the distal Humerus

Source page: https://510kreport.com/device/K132787
Methodology: https://510kreport.com/methodology