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Home » Nexxt Spine wins clearance for Matrixx stand-alone cervical implant

Nexxt Spine wins clearance for Matrixx stand-alone cervical implant

August 16, 2019 By Sean Whooley

Nexxt SpineNexxt Spine said last week that it won 510(k) clearance from the FDA for its Nexxt Matrixx stand-alone cervical system.

The anterior cervical interbody fusion system is used for the treatment of degenerative disc disease. The device will be used with the bone screw fixation provided and requires no additional fixation.

Nexxt Spine said it’s “eager to to release” the system into the market but did not indicate when.

“This enhancement of the Nexxt Matrixx portfolio was the next natural progression for Nexxt Spine,” president Andy Elsbury said in prepared remarks. “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.”

Filed Under: Food & Drug Administration (FDA), Orthopedics, Regulatory/Compliance, Spine Tagged With: Nexxt Spine

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About Sean Whooley

Sean Whooley is an associate editor who mainly produces work for MassDevice, Medical Design & Outsourcing and Drug Delivery Business News. He received a bachelor's degree in multiplatform journalism from the University of Maryland, College Park. You can connect with him on LinkedIn or email him at [email protected].

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