SpineUp’s Romero Cervical Cage Devices Receive the FDA’s 510(k) Clearance

SpineUp has been granted 510(k) clearance by the FDA for its Romero self-anchored cervical cage and its Romero cervical cage.

The devices are made of the newest version of Invibio’s polymers that promote better osteointegration. Designed to support the inward curve of the lower back, they are fixed in place with self-tapping and self-drilling screws.

The cervical cages are the Hollywood, Fla.-based company’s first two products. It is developing a range of sterile spinal implants intended to reduce the risk of infection, along with new instruments to simplify surgical techniques.