# K242141: TiLink-P SI Joint Fusion System

- Pathway: 510(k) (Special)
- Applicant: SurGenTec, LLC
- Decided: Aug 21, 2024 after 30 days
- Product code: OUR (Sacroiliac Joint Fixation)
- Device class: 2
- Regulation: 21 CFR 888.3040
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 19 generations back to K841189 (1984). 129 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 131 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K240720: TiLink-P SI Joint Fusion System, SurGenTec, LLC (2024) Summary page 5.

## Most influential descendants
- K243835: TiLink-P SI Joint Fusion System (2024), 0 descendants of its own

## Indications for use
The TiLink-P SI Joint Fusion System is intended for sacroiliac joint fusion for conditions including sacroiliac joint disruptions and degenerative sacroiliitis.

Source page: https://510kreport.com/device/K242141
Methodology: https://510kreport.com/methodology