Camber Spine Technologies received FDA 510(k) clearance and commenced U.S. launch of the SPIRAâ„¢ Open Matrix ALIF device, manufactured with additive techniques.Â
Xtant Medical received FDA 510(k) clearance for additional sizes of Calix-Câ„¢ cervical interbody cages, as well as use of the devices with allograft.Â