FDA accepted DiscGenics’ Investigational New Drug Application for a clinical study of its cell therapy product candidate to treat degenerative disc disease.
Spineology commenced full market release of the Eliteâ„¢ Expandable Interbody Fusion system. More than 300 cases have been completed since limited launch in 2Q16.Â
OrthAlign received CE Mark Approval to market the DAA HipAlign® Direct Anterior Approach Total Hip system and UniAlign® Unicompartmental Knee Arthroplasty.
K2M received FDA 510(k) clearance to market the YUKON™ OCT system to support fusion with posterior fixation in the occipito-cervico-thoracic spine.Â