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.

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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.

At the Becker’s 32nd Annual Meeting: The Business and Operations of ASCs, taking place October 29-31 in Chicago, ASC leaders, surgeons and healthcare executives will explore strategies to drive growth, enhance operational performance, navigate reimbursement challenges and prepare for the future of ambulatory surgery. Apply for complimentary registration now.

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