The line’s size expansion is expected to cover more than 80 percent of lumbar fusion patients. The device allows surgeons to perform lumbar interbody fusion while protecting the patient’s nerves, according to a news release.
Interventional Spine Receives FDA Clearance
Irvine, Calif.-based Interventional Spine has received FDA clearance for 11 additional sizes of its Opticage Expandable Interbody Fusion Device.
From repetitive to real-time: AI that lightens the back-office load
Recommended Live Webinar on Jan 22, 2026 12:00 PM - 1:00 PM CST