Interventional Spine Receives FDA Clearance for Spine Device

Interventional Spine, an Irvine, Calif.-based spine device company, has received FDA clearance for its Opticage Expandable Intervertebral Body Fusion device, according to a company news release.

Advertisement

The Opticage is part of Interventional Spine’s PerX360 System and can be used with the Optiport Access Instrument. The system is now the only system designed for surgeons to perform a complete percutaneous lumbar interbody fusion with two 15-mm incisions for treating lumbar discogenic pain.

Related Articles on Spine Devices:

Life Spine Reports 29% Revenue Growth in 2011

Choice Spine Launches Starfire Pedicle Screw System

Medtronic Receives FDA Clearance for Surgical Spine Device

At the Becker's 23rd Annual Spine, Orthopedic and Pain Management-Driven ASC + The Future of Spine Conference, taking place June 11-13 in Chicago, spine surgeons, orthopedic leaders and ASC executives will come together to explore minimally invasive techniques, ASC growth strategies and innovations shaping the future of outpatient spine care. Apply for complimentary registration now.

Advertisement

Next Up in Spinal Tech

  • From new technology acquisitions to regulatory clearances to leadership changes, here are 20 developments and updates from the biggest players…

  • SurGenTec’s ION-C earned FDA 510(k) clearance for ION-C navigation instruments with the ION-C posterior cervical facet fixation implant, according to…

  • VB Spine has made big pushes into the spine medtech space so far in 2026, including global expansions. Six headlines…

Advertisement

Comments are closed.