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The US FDA Has Granted 510(K) Clearance to Spine Wave's Intervertebral Body Fusion Device
May 2, 2013The 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
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