# K190143: LARS AC Band Device

- Pathway: 510(k) (Traditional)
- Applicant: Corin USA
- Decided: Nov 4, 2019 after 279 days
- Product code: HTN (Washer, Bolt Nut)
- 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: 8 generations back to K792022 (1979). 41 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 43 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K091207: Surgicraft Lockdown Acromioclavicular (AC) Device, Surgicraft, Ltd. (2011) Summary page 4.

## Most influential descendants
- K253115: Lars Acj (2026), 0 descendants of its own

## Indications for use
The LARS® AC Band device is indicated to provide fixation during the healing process following a syndesmotic trauma, such as fixation of acromioclavicular separations due to coracoclavicular ligament disruptions. The LARS® AC Band device is intended for single use only.

Source page: https://510kreport.com/device/K190143
Methodology: https://510kreport.com/methodology