Curiteva’s Inspire Porous 3D Printed Cervical System Cleared

The FDA has granted 510(k) clearance to Curiteva’s Inspire 3D Porous PEEK cervical interbody system with a structure that closely matches human cancellous bone — the “spongey” bone found at the end of long bones.

The device, an alternative to the titanium typically used in spinal surgeries, exhibits “superior mechanical strength” while achieving the elasticity of natural bone, the company said, adding that the device promoted cell attachment and healing in preclinical animal and in vitro studies.

Curiteva plans to launch the product in several academic centers in the U.S.