Accelus gets interbody fusion system FDA cleared

Accelus’ TiHawk 11 interbody device was cleared by the FDA.

Advertisement

TiHawk11 is part of the FlareHawk line of spinal fusion cages and has an expandable, 11mm-wide insertion profile, according to a May 12 news release. It is designed to increase stability and provide more space for bone grafts.

“By expanding on their family of TiHawk offerings to include this even larger footprint, Accelus has provided surgeons with a comprehensive set of devices for any transforaminal or posterior lumbar interbody fusion procedure,” Peter Derman, MD, a surgeon who helped develop the device, said in the release.

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

Advertisement

Comments are closed.