Zavation Medical Products LLC has announced FDA 510(k) clearance of its eZspand Lateral, an expandable lumbar interbody fusion device, according to a press release.
The eZspand Lateral device is an addition to Zavation’s eZspand interbody system, which is indicated for use with autogenous bone graft in spinal fusion procedures in skeletally mature patients who have had 6 months of nonoperative treatment, according to the release.
“Our product development team’s dedication to creatively blending simplicity and precision in a robust product design has produced an expandable