The 6 mm Titanium Cervical Fusion Spine Cage Set is a specialized cervical spinal implant system designed for professional use in cervical interbody fusion procedures. This orthopedic spine implant set combines 6 titanium cervical fusion cages with 14 fixation screws in 16 mm and 18 mm lengths, providing a comprehensive configuration for cervical spinal stabilization and fusion applications. The 6 mm cage profile is designed for use in appropriately prepared cervical intervertebral spaces according to the surgeon’s selected operative technique and patient-specific requirements.
Cervical interbody fusion cages are used following appropriate preparation of the intervertebral disc space as part of surgical procedures intended to stabilize the cervical spine. The cage provides structural support within the interbody space and is intended to help maintain the desired disc-space height and alignment while the fusion process develops. The 6 mm cervical fusion cage provides a defined implant height for cervical reconstruction applications where this size is appropriate based on preoperative imaging, intraoperative assessment, patient anatomy, and surgeon judgment.
The cages are manufactured from titanium, a material widely used in orthopedic and spinal implant technology. Titanium provides a combination of mechanical strength, durability, corrosion resistance, and established biocompatibility for implant applications. Its characteristics make titanium a commonly selected material for spinal fixation and interbody implant systems. The material also provides suitable imaging characteristics for postoperative evaluation when used according to accepted clinical practice.
The system includes 14 fixation screws in 16 mm and 18 mm lengths. The availability of different screw lengths allows the surgeon to select the appropriate fixation configuration according to the patient’s anatomy, implant position, surgical approach, and applicable device instructions. Correct screw selection and placement are essential considerations during cervical implant fixation and should be determined by a qualified spine surgeon.
The 6 mm titanium cervical fusion cage is designed to provide structural support and contribute to cervical interbody stabilization. Depending on the clinical indication and surgical technique, cervical interbody fusion may be performed following procedures such as decompression and removal of damaged disc material. The cage is positioned within the prepared disc space under appropriate surgical guidance, with fixation used where indicated by the specific implant system and operative technique.
The set configuration of 6 cervical cages and 14 fixation screws can provide a practical inventory of cervical implant components for hospitals, orthopedic surgery centers, spine surgery departments, and authorized medical device distributors. Maintaining multiple cages and fixation screws allows the surgical team to select the appropriate components for the procedure within the available implant range.
Proper handling of implantable medical devices is essential. The Cervical Fusion Spine Cage – 6 mm and associated fixation screws should be handled, stored, inspected, and implanted according to the manufacturer’s instructions for use and applicable medical-device regulations. Implantable components should not be reused unless they are specifically designated and validated by the manufacturer for reuse. Any reusable surgical instrumentation used during the procedure should undergo validated cleaning, disinfection, inspection, packaging, and sterilization processes according to the manufacturer’s instructions and healthcare-facility protocols.
The titanium construction supports long-term implant durability, while the defined 6 mm cage height and supplied screw lengths provide a specialized configuration for cervical fusion applications. The system is intended for professional medical use and should be selected based on appropriate patient assessment, imaging, anatomical considerations, surgical objectives, and the surgeon’s clinical expertise.
The Cervical Fusion Spine Cage – 6 mm – 6 pcs with 14 Screws (16 mm & 18 mm) – Titanium provides a purpose-built cervical interbody implant configuration for professional spinal surgery. With six titanium cages, fourteen fixation screws, and 16 mm and 18 mm screw options, the system is designed to support appropriate cervical fusion and stabilization procedures when used by qualified medical professionals according to the applicable device instructions.
Key Features
- 6 mm cervical fusion spine cage for cervical interbody fusion applications
- Manufactured from durable titanium for orthopedic implant use
- Complete set contains 6 cervical fusion cages
- Includes 14 cervical fixation screws
- Supplied with 16 mm and 18 mm screw lengths
- Designed for professional cervical spinal fusion procedures
- Supports interbody structural stabilization of the cervical spine
- Provides a defined 6 mm implant height for appropriate surgical applications
- Titanium offers strength, durability, corrosion resistance, and established biocompatibility
- Multiple screw lengths provide fixation options according to surgical requirements
- Suitable for professional orthopedic and spine surgery environments
- Intended for use by appropriately trained and qualified spinal surgeons
Product Specifications
| Specification | Details |
|---|---|
| Product Name | Cervical Fusion Spine Cage |
| Cage Height | 6 mm |
| Material | Titanium |
| Application | Cervical Interbody Fusion |
| Surgical Region | Cervical Spine |
| Number of Cages | 6 pcs |
| Number of Screws | 14 pcs |
| Screw Lengths | 16 mm & 18 mm |
| Implant Type | Cervical Interbody Fusion Cage |
| Fixation Type | Screw Fixation |
| Product Category | Orthopedic Spinal Implants |
| Intended Application | Cervical Spinal Stabilization and Fusion |
| Intended Users | Qualified Spine Surgeons / Medical Professionals |
FAQs
1. What is a 6 mm Cervical Fusion Spine Cage used for?
A 6 mm Cervical Fusion Spine Cage is an interbody spinal implant designed for cervical fusion procedures. It provides structural support within the prepared cervical intervertebral space and helps maintain the intended disc-space region during the fusion process.
2. What material is the 6 mm cervical fusion cage made from?
The cervical fusion cage is manufactured from titanium, a commonly used material for orthopedic and spinal implants due to its mechanical strength, durability, corrosion resistance, and established biocompatibility.
3. How many cages are included in this cervical fusion set?
The Cervical Fusion Spine Cage – 6 mm set includes 6 titanium cervical fusion cages.
4. How many fixation screws are included?
The set contains 14 fixation screws in total, with screw lengths of 16 mm and 18 mm.
5. What screw sizes are included with the cervical spine cage?
This cervical spine implant set includes 16 mm and 18 mm fixation screws. The appropriate screw length should be selected by the qualified surgeon based on patient anatomy, implant position, surgical technique, and applicable device instructions.
6. What is the difference between a 5 mm and 6 mm cervical fusion cage?
The primary dimensional difference specified in these products is the cage height. A 6 mm cage has a 1 mm greater height than a 5 mm cage. Selection should be based on the patient’s anatomy, prepared disc space, imaging, and the surgeon’s clinical and technical assessment.
7. Is this titanium cervical fusion cage intended for professional spinal surgery?
Yes. The system is designed for professional cervical interbody fusion and spinal stabilization applications and should be selected and implanted by an appropriately trained and qualified spine surgeon.
8. How should the cervical fusion cage be sterilized?
Implantable components should be handled according to the manufacturer’s validated instructions for use. Reusable surgical instruments associated with the procedure should be cleaned, inspected, packaged, and sterilized according to validated healthcare-facility procedures and the manufacturer’s instructions.
9. Can the 6 mm cervical fusion cage be reused?
Implantable components should not be reused unless the manufacturer specifically identifies and validates them for reuse. Single-use implant components should be managed according to applicable medical-device regulations and manufacturer instructions.

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