# K113602: Aap Loqteq Proximal Lateral Tibia Plate 4.5 System

- Pathway: 510(k) (Traditional)
- Applicant: Aap Implantate AG
- Decided: Oct 31, 2012 after 331 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 K023802 (2003). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K023802: Synthes 4.5 MM Titanium LCP Proximal Tibia Plating System, Synthes (Usa) (2003) Summary page 1.

## Indications for use
The aap LOQTEQ® Proximal Lateral Tibia Plates 4.5 System is intended for treatment of nonunions, malunions, and fractures of the proximal tibia, including simple, comminuted, lateral wedge, depression medial wedge, bicondylar combination of lateral wedge and depression, and fractures with associated shaft fractures.

Source page: https://510kreport.com/device/K113602
Methodology: https://510kreport.com/methodology