# K141823: Aap Loqtec Clavicle Plates 2.7/3.5

- Pathway: 510(k) (Traditional)
- Applicant: Aap Implantate AG
- Decided: Aug 7, 2014 after 31 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 K061753 (2006). 2 ancestors in all.
No later device cites it as a predicate yet.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K073186: Synthes 3.5MM LCP Clavicle Plate System, Synthes (Usa) (2007) Summary page 4.
- K061753: Synthes (Usa) Clavicle Hook Plates, Synthes (Usa) (2006) Summary page 4.

## Indications for use
The aap LOQTEQ® Clavicle Shaft Plate and aap LOQTEQ® Superior Lateral Clavicle Plate are intended for fixation of fractures, malunions, non-unions, and osteotomies of the clavicle. The aap LOQTEQ® AcroPlate is intended for fixation of lateral clavicle fractures and dislocations of the acromioclavicular joint.

Source page: https://510kreport.com/device/K141823
Methodology: https://510kreport.com/methodology