# K143490: VERTA Corpectomy Cage

- Pathway: 510(k) (Traditional)
- Applicant: Camber Spine
- Decided: Jan 26, 2015 after 49 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: 6 generations back to K003275 (2001). 6 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K072465: Niko Corpectomy Spacer, Globus Medical, Inc. (2007) Summary page 4.

## Most influential descendants
- K173800: Camber Spine Technologies SPIRA - V™ Open Matrix Corpectomy Cage (2018), 0 descendants of its own

## Indications for use
The VERTA Corpectomy Cage is a vertebral body replacement device intended for use in the thoracolumbar spine (T1-L5) to replace a collapsed, damaged, or unstable vertebral body due to tumor or trauma (i.e., fracture). The device is intended for use with bone graft and with supplemental fixation systems (such as anterior plating systems, or posterior screw systems) cleared for use in the spine.

Source page: https://510kreport.com/device/K143490
Methodology: https://510kreport.com/methodology