Interventional Spine Garners FDA Clearance
Irvine, Calif.-based Interventional Spine has gained FDA clearance for its 8-degree Lumbar Lordotic Opticage, joining the company’s family of FDA-cleared Opticage expandable interbody fusion devices.
The lumbar intervertebral body fusion device is cleared for use with autogenous bone graft in patients suffering from degenerative disc diseases at one or two contiguous levels from L2-S1.
The device alleviates pain by adjusting the pressure on the lower spine and can be implanted via posterior, transforaminal or lateral approach, according to the company. — Anisa Jibrell