Anterior Cervical Neogé Interbody Fusion Cage

Key Features

• PEEK-OPTIMA Polymer Construction: Made from medical-grade PEEK by Invibio, offering radiolucency for clear post-operative imaging assessment
• Titanium Alloy Markers: Incorporates Ti6Al4V ELI (Extra Low Interstitials) titanium alloy components for enhanced visibility on radiographic imaging
• Bone-Like Modulus: PEEK's elastic modulus closely matches that of cortical bone, reducing stress shielding and promoting natural load distribution
• Radiolucent Design: Allows for artifact-free X-ray, CT, and MRI imaging to assess fusion progress accurately
• Anatomical Profile: Designed to restore cervical disc height and maintain proper spinal alignment
• Biocompatible: Proven long-term biocompatibility with excellent clinical track record

Clinical Applications

• Anterior cervical discectomy and fusion (ACDF) procedures
• Treatment of cervical degenerative disc disease
• Management of cervical radiculopathy or myelopathy
• Single-level cervical spine fusion from C2 to T1
• Used in conjunction with autograft or allograft bone to facilitate fusion

Material Specifications

• Primary Material: PEEK (Polyetheretherketone) - PEEK-OPTIMA polymer
• Marker Material: Titanium Alloy Ti6Al4V
• Dimensions: 15mm (AP) x 6mm (Height)
• Compliance: Meets medical device regulatory standards (CE marked)

Benefits

• Immediate stability following discectomy
• Maintains intervertebral height and cervical lordosis
• Facilitates bone graft incorporation and fusion
• Reduces risk of graft site morbidity compared to autologous iliac crest harvest
• Superior puncture and compression resistance
• Long-term clinical success with proven fusion rates

Important Information

• Single-Use Device: For one-time use only
• Sterilization: Pre-sterilized and ready for surgical use
• Federal Law Restriction: This device is restricted by USA federal law to sale by or on the order of a physician
• Storage: Store in a cool, dry place away from direct sunlight