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.