MOD-C Cervical Implant
Spinal implant
An FDA-cleared cervical intervertebral body fusion device family for treating degenerative disc disease of the cervical spine from C2-T1, built from the company's CAMP biomaterial and scheduled for clinical launch in the second half of 2026.
- FDA 510(k) cleared for degenerative disc disease of the cervical spine (C2-T1)
- Built from CAMP calcium-acrylic modified polymer composite
- Microporous, hydrophilic structure similar to natural bone
- Enables ionic transfer at the implant interface
- Improved radiographic visibility versus legacy implant materials
Built for
Spine and orthopedic surgeons, hospitals, and surgical centers performing cervical fusion and other musculoskeletal reconstruction