Nexxt Spine’s latest additively manufactured spinal implant receives FDA clearance

Nexxt Spine's latest additively manufactured spinal implant receives FDA clearance
The Next Matrixx Stand Alone Cervical System has now received FDA 510(k) clearance (Courtesy Nexxt Spine)

Nexxt Spine LLC, a medical
device manufacturer based in Noblesville, Indiana, USA, has reported that
its Nexxt Matrixx® Stand Alone Cervical System, which was additively
manufactured on a GE Additive Concept Laser Mlab system, has received FDA
510(k) clearance and can now enter the market. 

The new 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. It
is intended to be used with the bone screw fixation provided and requires no
additional fixation.

“This enhancement of the
Nexxt Matrixx portfolio was the next natural progression for Nexxt Spine,”
stated Andy Elsbury, President, Nexxt Spine. “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.”

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