Low-profile expandable lumbar interbody device gets FDA nod

Spinal Tech

Spine device company MiRus received FDA 510(k) clearance for its IO expandable lumbar interbody, the company announced Aug. 31.

The device can be used in posterior and transforaminal lumbar interbody fusions. It has the lowest insertion profile of 4mm and the greatest expansion of 18mm.

The FDA clearance allows the interbody to be used in skeletally mature patients with degenerative disc disease at one or two contiguous levels in the lumbar spine.

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