Zero-profile Cervical Fusion PEEK Cage with Locking Screws

Category

An all-in-one anterior cervical interbody fusion device crafted from biocompatible PEEK polymer. Features an integrated zero-profile design with self-retaining locking screws for immediate stabilization. Eliminates the need for a separate plate, offering simplified insertionenhanced biomechanical stability, and reduced soft tissue irritation. Components include the PEEK spacer and titanium alloy locking screws.

Zero-Profile Cervical Fusion PEEK Cage with Locking Screws
Precision Engineering for Optimal Cervical Fusion

 

Product Overview:

This innovative cervical fusion device combines a radiolucent PEEK (Polyetheretherketone) interbody spacer with integrated titanium alloy locking screws in a single, zero-profile implant. Designed to streamline anterior cervical discectomy and fusion (ACDF) procedures, it eliminates traditional plating systems while providing immediate fixation and stability.

 

Key Specifications:

  • Materials: Bioinert PEEK polymer spacer; Titanium alloy (Ti-6Al-4V) locking screws.
  • Sizes: Multiple footprints (e.g., 14–18mm) and heights (e.g., 4–7mm) for C2–T1 anatomy.
  • Design: Monobloc spacer with pre-angled screw trajectories; Self-distracting leading edge; Self-locking screw mechanism.

 

Intended Use:

Indicated for single-level cervical fusion (C2–T1) in skeletally mature patients with:
  • Degenerative Disc Disease (DDD)
  • Cervical Spondylosis
  • Herniated Nucleus Pulposus
  • Spinal Stenosis
  • Deformity/Instability Correction

 

Clinical Advantages:

  1. Zero-Profile Design: Minimizes implant prominence and reduces dysphagia risk.
  2. All-in-One Solution: Combines fusion cage and fixation without auxiliary plating.
  3. PEEK Biomaterial: Modulus elasticity similar to bone (reduces stress-shielding); MRI/CT compatible.
  4. Locking Screw Technology: Screws lock into the spacer, preventing back-out and offering immediate stability.
  5. Simplified Technique: Reduced operative steps and instrumentation vs. plate-cage systems.
  6. Optimized Fusion: Graft chamber permits autologous/allograft bone packing.

 

Contraindications:

  • Active systemic infection or localized infection at surgical site
  • Osteoporosis, metabolic bone disease, or inadequate bone stock
  • Sensitivity to implant materials (PEEK/titanium alloy)
  • Multi-level fusion requirements
  • Pregnancy or pediatric patients
  • Morbid obesity (BMI >40) or conditions compromising wound healing

RX Only: This device requires specialized surgical training. Strictly adhere to operative technique guidelines. Potential risks include implant migration, non-union, vascular/neural injury, and screw-related complications.
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