# K233972: Camber Sacroiliac (SI) Fixation System

- Pathway: 510(k) (Traditional)
- Applicant: Camber Spine Technologies
- Decided: Feb 27, 2024 after 74 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: 17 generations back to K841189 (1984). 125 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 127 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K161210: RIALTO (TM) SI Fusion System, Medtronic Reusable Instruments for Use with the IPC (TM) Powerease (TM) System, and Medtronic Navigated Manual Reusable Instruments for use with the StealthStation (TM) and IPC (TM) Powerease (TM) Systems, Medtronic Sofamor Danek (2016) Summary page 4.
- K203503: Camber Sacroiliac (SI) Fixation System, Camber Spine Technologies, LLC (2022) Summary page 4.

## Most influential descendants
- K250247: panaSIa SI Fusion System (2025), 0 descendants of its own

## Indications for use
The Camber Sacroiliac (SI) Fixation System is intended for sacroiliac joint fusion for conditions including sacroiliac joint disruptions and degenerative sacroiliitis.

Source page: https://510kreport.com/device/K233972
Methodology: https://510kreport.com/methodology