# K173800: Camber Spine Technologies SPIRA - V™ Open Matrix Corpectomy Cage

- Pathway: 510(k) (Traditional)
- Applicant: Camber Spine Technologies
- Decided: Feb 2, 2018 after 50 days
- Product code: MQP (Spinal Vertebral Body Replacement Device)
- Device class: 2
- Regulation: 21 CFR 888.3060
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 7 generations back to K003275 (2001). 10 ancestors in all.
No later device cites it as a predicate yet.
0 of 11 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K143490: VERTA Corpectomy Cage, Camber Spine (2015) Summary page 4.
- K012254: VBR, Osteotech, Inc. (2001) Summary page 4.
- K010530: Geo Structure, Interpore Cross Intl. (2001) Summary page 4.

## Indications for use
The Camber Spine Technologies SPIRA-V™ Open Matrix Corpectomy Cage is indicated for use in the Thoracolumbar Spine (T1-L5) to replace collapsed, damaged, or an unstable vertebral body due to tumor or trauma (i.e., fracture). The Camber Spine Technologies SPIRA-V™ Open Matrix Corpectomy is intended to be used with additional FDA-cleared supplementary fixation systems. The Camber Spine Technologies SPIRA-V™ Open Matrix Corpectomy Cage system must be used with autogenous graft material.

Source page: https://510kreport.com/device/K173800
Methodology: https://510kreport.com/methodology