Superior anterior cervical fixation infused with Hydroxyapatite for faster bone growth.
Now available in a 12mm x 15mm footprint
What’s so new and great about Arena-C HA? We decided to integrate the entire interbody with a bone growth promoting material called hydroxyapatite (HA). This revolutionary new biomaterial, PEEK OPTIMA® HA Enhanced, drastically improves contact between the implant and the vertebral bodies.
Additionally, We’ve integrated HA througout the entire implant instead of simply coating contact surfaces. These features combine to help better encourage reliable bone formation and promote faster bony fusion.
Large Graft Volume
Arena-C HA’s enlarged bone graft window takes full advantage of this interbody’s solid construction, providing a large pocket for graft volume, and a better chance for bony fusion.
Improved Bone Contact
High degree of bone contact early in the healing process.
Perfect Pairing with Inset®
SpineFrontier’s low-profile Inset® anterior cervical plate plate contours to the Arena-C HA final construct.
Simple Instrumentation Set
Slim instrumentation allows the surgeon maximum visibility and control in an area of tight clearance. It’s ideal for letting the surgeon deliver the interbody through small incisions.
Bulleted Nose Design
A sleek design minimizes tissue disruption and procedure time.
Raised teeth grip firmly to the neighboring vertebral bodies, ensuring long-term fixation.
PEEK-OPTIMA® HA Enhanced By the Numbers
New Bone Formation
Micro CT analysis of the quality of new bone formation in the fusion, as well as the device surfaces 1*
Quality of New Bone Bridging
Micro CT analysis of the quality of new bone formation bridging in the fusion as well as the device surfaces 1*
EnHAnce your offerings.
Interested in using our technology? Just want to learn more? We’re eager to speak with you about your surgical needs and how our team can best support you.
The SpineFrontier Arena-C® HA PEEK Cervical Intervertebral Body Fusion Device is a spinal intervertebral body fusion device intended for intervertebral body fusion of the spine of skeletally mature patients, using autogenous bone graft to facilitate fusion. The device is indicated for use in patients with degenerative disc disease (DDD) of the cervical spine at one disc level from the C2-C3 disc to the C7-T1 disc.
The SpineFrontier® Arena-C® HA PEEK Cervical Intervertebral Body Fusion Device is intended to be used with supplemental spinal fixation system(s) cleared for use in the cervical spine (example: Anterior Cervical Plate Fixation). Degenerative disc disease is defined as discogenic pain with degeneration of the disc confirmed by history or radiographic studies. These patients should be skeletally mature and have had six (6) weeks of non-operative treatment prior to treatment with an intervertebral cage.