# K133675: Aap Loqteq Distal Anterolateral Tibia Plate 3.5

- Pathway: 510(k) (Traditional)
- Applicant: Aap Implantate AG
- Decided: Jan 23, 2014 after 55 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: 3 generations back to K882831 (1988). 9 ancestors in all.
No later device cites it as a predicate yet.
0 of 10 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K092812: Synthes (Usa) 2.7MM/ 3.5MM LCP Anterolateral Distal Tibia Plates, Synthes (Usa) (2010) Summary page 1.

## Indications for use
The aap LOQTEQ® Distal Anterolateral Tibia Plate 3.5 is indicated for fractures. osteotomies, and non-unions of the distal tibia, especially in osteopenic bone.

Source page: https://510kreport.com/device/K133675
Methodology: https://510kreport.com/methodology