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HD LifeSciences Receives 510(k) Clearance for HIVE(tm) ALIF Standalone System

Updated: Feb 2, 2021

MAY 12, 2020

HD LifeSciences has received 510(k) clearance from the U.S Food and Drug Administration (FDA) for its Hive(tm) ALIF Standalone Lumbar Interbody Fusion System. The patented implant system features a modular anterior portion that allows surgeon choice and flexibility in using integrated zero-profile fixation or anterior plating. The implant also features a patent-pending mechanism that allows the surgeon to adjust the footprint of the device pre-implantation to better match patient anatomy.

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