VGI Medical’s VerteLP Lateral Lumber Cage System receives FDA approval: 4 key notes

VGI Medical received FDA 510(k) clearance to market its VerteLP Lateral Lumber Cage System.

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Here are four key notes:

 

1. The system is intended for use during lateral lumbar fusion and features enhanced bi-cortical plating technology.

 

2. The VerteLP cage and integrated plating are delivered in the plane of the disc through a minimally invasive direct lateral approach.

 

3. The system was developed in consultation with a surgeon team led by David Greenwald, MD, of Flagler Brain & Spine Institute in St. Augustine, Fla.

 

4. VGI Medical was founded in 2007 and it focuses on developing unique spine devices and instrumentation.

 

More articles on devices:
MidCap Business Credit becomes SpineFrontier’s lending partner — 3 quick notes
OrthAlign to launch OrthAlign Plus for direct anterior hip replacement — 4 things to know
Burton’s new Outpatient LED Examination Light has arrived

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