# K121494: Loqteq Distal Lateral Femur Plate 4.5 (Left and Right Version) Loqreq Cortical Screw 4.5 T25, Self-Tapping

- Pathway: 510(k) (Traditional)
- Applicant: Aap Implantate AG
- Decided: Nov 19, 2012 after 182 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 K062564 (2006). 1 ancestor in all.
2 later devices descend from it; 1 cites it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K062564: Synthes LCP Distal Femur Plates, Synthes (Usa) (2006) Summary page 1.

## Most influential descendants
- K210043: LOQTEQ Distal Lateral Femur Plate 4.5 System (2021), 1 descendant of its own
- K232115: TDM Large Bone Plate and Screw System (2024), 0 descendants of its own

## Indications for use
The aap LOQTEQ6 Distal Lateral Femur Plate 4.5 System include plates for the left and right human femur. The plates accept 4.5 MM locking screws, 4.5 mm cortical screws and 4.5 mm periprosthetic screws. They are intended for: Buttressing multifragmentary distal femur fractures including: supracondylar, intra-articular and extra-articular condylar, periprosthetic fractures; fractures in normal or osteopenic bone; non-unions and malunions ; and osteotomies of the femur

Source page: https://510kreport.com/device/K121494
Methodology: https://510kreport.com/methodology