Broader FDA Clearance for Spineology Elite Expandable Interbody Fusion System

Spineology received expanded FDA 510(k) clearance of the Elite Expandable Interbody Fusion to include a narrower 10mm version of the device and an indication for use with allograft bone, such as Incite cortical fibers.

Elite completed limited launch in early 4Q16.

Sources: Spineology, Inc.; ORTHOWORLD Inc.

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Julie Vetalice is ORTHOWORLD's Editorial Assistant. She has covered the orthopedic industry for over 20 years, having joined the company in 1999.

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