Nexxt Spine received FDA 510(k) clearance to market the NEXXT MATRIXX® Stand Alone Cervical System, an addition to its portfolio of 3D-printed porous titanium interbodies.
The device is indicated as an adjunct to fusion at one or two contiguous levels in skeletally mature patients for the treatment of degenerative disc disease, and is to be used with bone graft. It requires no additional fixation, and comes in a range of footprints with screws for one-step locking. The implant is contained within the excised disc space and is designed not to protrude past the mid-line edge of the vertebral body, reducing the potential for soft tissue damage or irritation.
NEXT MATRIXX implants comprise a 3D-printed cellular titanium scaffold and tailored surface topology. The line includes a devices for cervical, TLIF, TLIF Oblique and vertebral body replacement applications.
Source: Nexxt Spine LLC