Anterior Cervical Interbody Fusion Cage (PEEK) - AP 13-H 7mm
Anterior cervical interbody fusion cage for surgical treatment of cervical spine disorders. Made from PEEK-OPTIMA biocompatible polymer, this implant replaces damaged intervertebral discs and promotes fusion between vertebral bodies while restoring disc height and proper cervical alignment. Inserted through anterior neck approach with hollow central chamber for bone graft material.
Key Features: PEEK-OPTIMA construction, radiolucent for clear CT/MRI imaging, radiopaque markers for X-ray verification, pyramidal teeth prevent migration, central graft cavity, 7mm height.
Specifications: Material: Polyetheretherketone (ASTM F2026), Height: 7mm, Single-use sterile, Requires specialized instruments, CE Class IIb.
Indications: Degenerative disc disease (C2-T1), cervical radiculopathy/myelopathy, herniated discs, post-traumatic instability, revision surgery, spondylosis with stenosis.
Contraindications: Active infection, severe osteoporosis, tumor at site, PEEK allergy, immature skeleton.
Prescription Required: Yes
Safety Notes: Implantation by qualified spine surgeon only. Requires proper patient selection. Risk of subsidence with poor bone quality. May need supplemental plate fixation. Follow post-operative protocols. Regular radiographic monitoring essential.
Variations: Multiple heights (5-10mm), various footprints/angles, stand-alone with screws, titanium-coated options, expandable designs.
Product Links:
- https://www.medicalexpo.com/medical-manufacturer/peek-interbody-fusion-cage-55097.html
- https://www.prodorth.com/cervical-peek-cages
- https://www.czmeditech.com/Cervical-Peek-Cage-pd42297070.html
Disclaimer: For inventory identification and medical professional reference only. This device must only be used by qualified surgeons trained in spinal fusion techniques. Consult manufacturer's instructions for use, patient selection criteria, and complete safety information. Check local regulations, sterilization status, and expiration dates before distribution. Not for direct patient use without proper medical evaluation and surgical planning.