FDA clears Camber Spine Technologies' anterior interbody fusion system: 3 key notes

Spinal Tech

Camber Spine Technologies' ENZA Zero Profile Anterior Interbody Fusion system received FDA 510(k) clearance.

Here are three key notes:


1. The system is a minimally invasive interbody fusion device providing integrated fixation.


2. The system is designed for use in patients with degenerative disc disease at 1 or 2 contiguous levels from L2 to S1.


3. The system is intended for use with bone graft and with supplemental fixation systems.


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