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.

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