# K141246: Life Spine Sacroiliac Joint Fixation System

- Pathway: 510(k) (Traditional)
- Applicant: Life Spine, Inc.
- Decided: Feb 22, 2015 after 284 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: 6 generations back to K903810 (1990). 11 ancestors in all.
29 later devices descend from it; 7 cite it directly.
0 of 41 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K112028: SI-Lok Sacroiliac Joint Fixation System, Globus Medical, Inc. (2011) Summary page 4.

## Most influential descendants
- K180749: Life Spine SIMPACT Sacroiliac Joint Fixation System (2018), 14 descendants of its own
- K201538: Life Spine SIMPACT Sacroiliac Joint Fixation System (2020), 13 descendants of its own
- K153656: PathLoc-SI Joint Fusion System (2016), 13 descendants of its own
- K181600: PathLoc-SI Joint Fusion System (2018), 11 descendants of its own
- K210035: ZESPIN SI Joint Fusion System, MegaCerfix Posterior Cervical Fixation System, MegaCerfix Anterior Cervical Plate System, Spinema Lumbar Plate System (2021), 10 descendants of its own

## Indications for use
The Life Spine Sacroiliac Joint Fixation System is intended for sacroiliac joint fusion for conditions including sacroiliac joint disruptions and degenerative sacroiliitis.

Source page: https://510kreport.com/device/K141246
Methodology: https://510kreport.com/methodology