Accelus gets interbody fusion system FDA cleared

Carly Behm -  

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

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.

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