# K170843: Alians Fragment Specific

- Pathway: 510(k) (Traditional)
- Applicant: Newclip Technics
- Decided: Jun 16, 2017 after 87 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: 14 generations back to K962616 (1996). 151 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 153 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K142906: APTUS Wrist 2.5 System, Medartis AG (2015) Summary page 5.
- K060041: Trimed Bone Plates, TriMed, Inc. (2006) Summary page 5.
- K102694: 2.4MM VA-LCP Dorsal Distal Radius Plates, Synthes (Usa) (2010) Summary page 5.
- K130774: Universal Distal Radius System, Newclip Technics (2013) Summary page 5.
- K161448: Footmotion Plating System, Newclip Technics (2016) Summary page 5.
- K143061: Activ Ankle Locking Plating System, Newclip Technics (2015) Summary page 5.

## Most influential descendants
- K213214: Xpert Wrist (2021), 0 descendants of its own

## Indications for use
The Alians Fragment Specific range is intended for hand and forearm fractures, osteotomies and arthrodeses in adults.

Source page: https://510kreport.com/device/K170843
Methodology: https://510kreport.com/methodology