# K153034: aap LOQTEQ VA Radius Set 2.5

- Pathway: 510(k) (Traditional)
- Applicant: Aap Implantate AG
- Decided: Jan 21, 2016 after 94 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: 6 generations back to K962616 (1996). 25 ancestors in all.
No later device cites it as a predicate yet.
0 of 26 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K102694: 2.4MM VA-LCP Dorsal Distal Radius Plates, Synthes (Usa) (2010) Summary page 4.
- K070946: Synthes LCP Diaphyseal-Metaphyseal (Dia-Meta) Volar Distal Radius Plates, Synthes (Usa) (2007) Summary page 4.
- K083694: Synthes (Usa) 2.4 MM VA-LCP Two Column Volar Distal Radius Plates, Synthes (Usa) (2009) Summary page 4.
- K103332: Aptus Ulna Plates, Medartis AG (2011) Summary page 4.

## Indications for use
LOQTEQ® VA Volar Distal Radius Plate 2.5, LOQTEQ® VA Distal Radius Straight Plate 2.5, LOQTEQ® VA Distal Radius L-Plate 2.5 « Fixation of complex intra-articular and extra-articular fractures and osteotomies of the distal radius LOQTEQ® VA Distal Ulna Plate 2.5, LOQTEQ® VA Distal Ulna Hook Plate 2.5 « Fractures and osteotomies of the distal ulna

Source page: https://510kreport.com/device/K153034
Methodology: https://510kreport.com/methodology