The US Food and Drug Administration (FDA) has granted 510(k) clearance to Spine Wave's intervertebral body fusion device. Producing expandable PEEK spacers, the StaXx IB system will now for the first time offer an expandable device with ...
Tags: FDA, Spine Wave
The US Food and Drug Administration (FDA) has approved an expanded indication for use of Integra LifeSciences' Vu aPOD Prime intervertebral body fusion device (IBD) in anterior lumbar interbody fusion (ALIF) procedures. The Vu aPOD Prime ...
Tags: intervertebral body fusion device, supplemental fixation implants