Interventional Spine’s lumbar intervertebral body fusion device receives FDA clearance

Interventional Spine received U.S. Food and Drug Administration clearance for its Lateral Opticage Expandable Intervertebral Body Fusion Device.

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The lumbar intervertebral body fusion device is indicated for use with autogenous bone graft in patients with degenerative disc disease at one or two contiguous levels from L2-S1. It can be implanted via posterior, transforaminal or lateral approach.

 

The device is a part of Interventional Spine’s family of Opticage Expandable Interbody Fusion Devices cleared for TLIF earlier this year.

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