# K181228: IlluminOss Bone Stabilization System

- Pathway: 510(k) (Traditional)
- Applicant: Illuminoss Medical, Inc.
- Decided: Aug 31, 2018 after 115 days
- Product code: QAD (Rod, Fixation, Intramedullary And Accessories, In-Vivo Cured, Light-Activated)
- Device class: 2
- Regulation: 21 CFR 888.3023
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K183145: IlluminOss Photodynamic Bone Stabilization System (2018), 0 descendants of its own

Source page: https://510kreport.com/device/K181228
Methodology: https://510kreport.com/methodology