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

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

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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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RTI Surgical outlines why stockholders should elect its director nominees on WHITE proxy card: 5 points
Stryker, Smith & Nephew, K2M & more: 18 key notes

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