HD LifeSciences gains FDA clearance for lumbar interbody fusion system

Spinal implant developer HD LifeSciences on May 12 achieved FDA 510(k) clearance for its Hive anterior lumbar interbody fusion system.

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Three things to know:

1. Hive ALIF is designed with a modular anterior portion that allows spine surgeons to choose between using zero-profile fixation or anterior plating.

2. The device enables surgeons to adjust the footprint before implantation to better match patient anatomy.

3. Hive ALIF features a variety of implant configurations with multiple lordotic choices to accommodate patient needs. 

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