FDA Clears Benvenue’s Expandable Interbody Device

The FDA has handed Benvenue 510(k) clearance for its Luna XD expandable interbody device for use in patients with symptomatic degenerative disc disease (DDD).

The minimally invasive device is placed via a small incision and gives the patient’s spine anterior column stability, strength and fusion.

The implant offers surgeons a large graft chamber to allow for successful fusion, maximum height restoration and good sagittal balance.