FDA Clears HD LifeSciences’ Lumbar Interbody Fusion System

HD LifeSciences has received FDA 510(k) clearance for its Hive ALIF standalone lumbar interbody fusion system, an adjustable spinal implant.

The implant technology enables surgeons to choose between integrated zero-profile fixation or anterior plating and can be adjusted prior to implantation to better fit patient anatomy.

The Hive ALIF system offers surgeons a number of configurations for height, width, depth and lordotic choices, the company said.