CERVICAL CAGE SYSTEM

ACDF Cage Spacer 0° Deg. – Peek – Sterile
ACDF Cage Spacer peek
ACDF Cage Spacer 0° Deg. – Peek – Sterile
ACDF Standalone Cage PRO 7° Deg. Taper -Titanium
ACDF Standalone Cage PRO 0° Deg. Taper – Peek (Sterile)
ACDF Standalone Cage Implant Set – Titanium
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Product Overview
TLIF Cage System

TLIF Cage System

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An Anterior Cervical Discectomy and Fusion (ACDF) System is a specialized spinal implant solution used to stabilize the cervical spine following decompression procedures. It involves the removal of a damaged intervertebral disc and is replaced with an interbody cage, often used in combination with an anterior cervical plate and screws to provide structural support.

This construct helps restore disc height, maintain cervical alignment, and relieve neural compression while promoting solid bony fusion between adjacent vertebrae. ACDF systems are commonly used in the treatment of degenerative disc disease, cervical spondylosis, trauma, and deformities.

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Product DESCRIPTION

The Anterior Cervical Discectomy and Fusion (ACDF) System by Siora Surgicals Pvt. Ltd. is a precision-engineered spinal solution designed to stabilize the cervical spine following decompression procedures. It is used to restore disc height, maintain cervical alignment, and promote solid bony fusion between adjacent vertebrae through an anterior approach.

Manufactured from high-quality, biocompatible materials — including PEEK, Titanium (Ti-6Al-4V ELI), and 3D porous Titanium — the ACDF system combines mechanical strength, durability, and excellent imaging compatibility. Its anatomical, zero-profile design minimizes soft tissue irritation while ensuring optimal implant performance and patient comfort.

The system offers hybrid zero-profile cages, zero-profile cages with screws, and standalone cage options providing flexibility across different surgical techniques. It is available in heights ranging from 6 mm to 12 mm (in 1 mm increments), with a footprint of 14 mm × 16 mm, and lordotic options of 0° and 7° to accommodate varying patient anatomies. The system incorporates 4.0 mm self-drilling, self-tapping screws with a locking mechanism, ensuring secure fixation, reducing screw back-out, and supporting standalone procedures.

Designed for ease of insertion and precise implant positioning, the ACDF system enables effective decompression of neural elements while maintaining structural integrity of the cervical spine. Backed by stringent manufacturing standards, Siora Surgicals Pvt. Ltd. ensures consistent quality, dependable performance, and reliable clinical outcomes in anterior cervical spine procedures.

PRODUCT FEATURES

1. Standalone & Zero-Profile Design

  • Integrated cage-plate functionality allows the implant to function as a standalone device, eliminating anterior plate prominence and reducing soft tissue irritation and dysphagia risk.

2. Versatile Cage Configurations

  • Hybrid zero-profile, zero-profile with integrated screws, and standalone cages provide flexibility across different surgical techniques with reliable fixation and simplified procedures.

3. Anatomical Lordotic Geometry

  • Pre-contoured design (0° and 7° lordosis) restores natural cervical alignment, improves disc height, and supports stable fusion.

4. Secure Locking & Fixation System

  • Self-locking screws with Titanium (Ti-6Al-4V ELI) interface ensure secure fixation, resist loosening, and minimize the risk of screw back-out while maintaining construct stability.

5. Optimized Screw Angulation

  • 53° screw trajectory with ±5° cranial-caudal variation enables secure bone engagement, balanced load distribution, and enhanced construct stability.

6. Optimized Anatomical Footprint

  • 16 mm × 14 mm footprint maximizes endplate contact, improves load transfer, and ensures precise anatomical fit within cervical vertebrae. 
CLINICAL INDICATIONS

The Anterior Cervical Interbody Fusion Cage System is indicated for the treatment of cervical spine conditions using an anterior approach, typically between C3 and C7, including:

1. Degenerative Disc Disease (DDD)

  • Symptomatic disc degeneration causing pain, disc height loss, and neural compression, requiring decompression, disc replacement, and interbody fusion.

2. Cervical Radiculopathy and Myelopathy

  • Nerve root or spinal cord compression due to disc herniation or degenerative changes, requiring anterior Decompression and stabilization.

3. Cervical Spondylosis and Trauma

  • Degenerative changes or traumatic injury leading to disc collapse, osteophyte formation, or instability, requiring restoration of disc height, anterior column support, and interbody fusion with stabilization using standalone or integrated fixation constructs.

4. Revision Procedures / Failed Previous Surgery

  • Persistent or recurrent symptoms following prior cervical procedures, requiring re-decompression and fusion with enhanced fixation options.

5. Pseudarthrosis or Cervical Deformities (e.g., Kyphosis)

  • Non-union after prior fusion or abnormal cervical alignment requiring corrective stabilization and interbody fusion.
Available Sizes
Cat No.Length (mm)Deg.
Ti.1206.606 – Ti.1206.612 (Titanium)6 – 12
Ti.1206.706 – Ti.1206.712 (Titanium)6 – 12
ST.1206.606 – ST.1206.612 (Peek)6 – 12
ST.1206.706 – ST.1206.712 (Peek)6 – 12
Cat No.Length (mm)Deg.
Ti.1206.206 – Ti.1206.212 (Titanium)6 – 12
Ti.1206.306 – Ti.1206.312 (Titanium)6 – 12
ST.1206.206 – ST.1206.212 (Peek)6 – 12
ST.1206.306 – ST.1206.312 (Peek)6 – 12
Cat No. (Titanium)Dia (mm)Length (mm)
Ti.1206.410 – Ti.1206.4204.010 – 20
Cat No. (Titanium)Dia (mm)Length (mm)
Ti.1206.510 – Ti.1206.5204.010 – 20

frequently asked questions

What is the Anterior Cervical Interbody Fusion (ACDF) Cage System used for?

The ACDF Cage System is used to restore disc height and stabilize the cervical spine (C3–C7) following anterior cervical discectomy procedures. It helps maintain spinal alignment, decompress neural elements, and promote solid bony fusion between adjacent vertebrae.

The system is manufactured from high-quality, biocompatible materials including PEEK, Titanium (Ti-6Al-4V ELI), and 3D porous Titanium, ensuring strength, durability, and excellent imaging compatibility. It is sterilized using gamma radiation (ISO 11137), ensuring residue-free sterility in sealed packaging.

The system offers hybrid zero-profile cages, zero-profile cages with integrated screws, and standalone cage options. It includes 4.0 mm self-drilling and self-tapping screws with a locking mechanism, providing enhanced fixation stability and supporting standalone applications without the need for additional anterior plating in selected cases.

Yes. Siora Surgicals offers OEM/ODM services, supports global distribution, and partners with distributors worldwide for spinal implant solutions.

Siora Surgicals provides complete export support, including sterile processing, documentation, packaging, and reliable logistics coordination to ensure timely global delivery.

Siora provides technical support, product training, and clinical guidance to ensure proper usage and optimal surgical outcomes.

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