August 5, 2019- Noblesville, IN-  Nexxt Spine LLC, a pioneer in the design and manufacturing of innovative spinal solutions, is pleased to announce the FDA 510(k) clearance of the NEXXT MATRIXX® Stand Alone Cervical System.  Born from engineering excellence, the system encompasses the cutting-edge design and surgeon friendly precision distinct to the NEXXT MATRIXX® brand of 3D printed porous titanium interbodies.

The NEXXT MATRIXX® Stand Alone Cervical System is a stand-alone anterior cervical interbody fusion system intended for use as an adjunct to fusion at one or two contiguous levels (C2-T1) in skeletally mature patients for the treatment of degenerative disc disease.  The NEXXT MATRIXX® Stand Alone Cervical System is intended to be used with the bone screw fixation provided and requires no additional fixation.

The addition of Stand Alone Cervical to a preexisting lineup of world class Nexxt Spine solutions comes with great industry enthusiasm.  Recognized for marrying design expertise and quality manufacturing, the company touts product features unique to the industry.  Having mastered the trifecta of tailored surface topography, cellular scaffolding and bone biology relevance, Nexxt Spine is eager to release Stand Alone Cervical into the market.

“This enhancement of the NEXXT MATRIXX® portfolio was the next natural progression for Nexxt Spine,” states President Andy Elsbury.  “With patient care always top of mind, we strive to develop end products that surgeons prefer and hardware patients can count on.  Our Stand Alone Cervical is no exception and will showcase the propensity of NEXXT MATRIXX® technology to facilitate the body’s natural power of cellular healing for fortified fusion.”