| Available Heights | 4 mm, 5 mm, 6 mm, 7 mm, 8 mm, 9 mm Height |
| Material | PEEK |
| Qualification | CE / ISO13485 / NMPA |
| Package | Sterile Packaging 1pcs/package |
| MOQ | 1 Pcs |
| Supply Ability | 1000+ Pieces per Month |
To achieve proper sagittal alignment
Facilitates vascularization
Allow for visualization and implant placement verification.
Prevent implant migration
Allows more area for bone graft-to-endplate contact
There are several contraindications to consider before undergoing Cervical Interbody Cage (CIC) placement. These contraindications may include:
It is important to note that these contraindications may vary depending on the individual patient and their specific medical condition. It is always best to consult with a qualified healthcare professional to determine the suitability of CIC placement based on the patient's unique circumstances.
The cage is manufactured from biocompatible PEEK (polyetheretherketone) and is equipped with integrated tantalum markers to facilitate precise visualization and implant placement verification under fluoroscopy.
To accommodate diverse patient anatomies and disc space requirements, the implant is provided in 6 distinct heights: 4 mm, 5 mm, 6 mm, 7 mm, 8 mm, and 9 mm.
The device features a trapezoid anatomical shape to restore lordosis, pyramidal teeth to prevent implant migration, lateral openings to facilitate vascularization, and a large center opening allowing substantial bone graft-to-endplate contact.
Contraindications include active or systemic infections, severe osteoporosis, known allergies or sensitivities to implant materials (such as PEEK), insufficient bone quality or quantity, and unrealistic patient recovery expectations.
Each Cervical Interbody Cage is supplied in individual sterile packaging (1 pcs/package). It complies with international quality standards backed by CE, ISO13485, and NMPA certifications, with an MOQ of 1 piece and a monthly supply capacity exceeding 1,000 pieces.