Cervical anterior plate (ACP) is a medical device used in spinal surgery specifically for stabilizing the cervical spine. The Spinal Anterior Cervical Plate is designed for implantation in the anterior part of the cervical spine, providing necessary support during the healing process after discectomy or spinal fusion surgery.
The main function of spinal cervical anterior plate is to enhance the stability of the cervical spine after surgery. When the intervertebral disc is removed or fused, the vertebrae may become unstable, leading to potential complications. The anterior cervical plate (ACP) is like a bridge that connects the vertebrae together, ensuring their correct alignment and promoting healing. It is usually made of biocompatible materials such as titanium or stainless steel to ensure good integration with the body and minimize the risk of rejection.
| Component / Parameter | Specification Details |
|---|---|
| Shielder ACP Plate | 4 holes: 19.0 mm, 21.0 mm, 23.0 mm, 25.0 mm, 27.5 mm, 30.0 mm length |
| 6 holes: 32.5 mm, 35.0 mm, 37.5 mm, 40.0 mm, 42.5 mm, 45.0 mm, 47.5 mm, 50.0 mm length | |
| 8 holes: 52.5 mm, 55.0 mm, 57.5 mm, 60.0 mm, 62.5 mm, 65.0 mm, 67.5 mm, 70.0 mm, 72.5 mm length | |
| 10 holes: 75.0 mm, 77.5 mm, 80.0 mm length | |
| Shielder Variable Angle Self-tapping Screw | Ф4.0 x 10 mm, 12 mm, 14 mm, 16 mm, 18 mm, 20 mm |
| Ф4.5 x 10 mm, 12 mm, 14 mm, 16 mm, 18 mm, 20 mm | |
| Shielder Variable Angle Self-drilling Screw | Ф4.0 x 10 mm, 12 mm, 14 mm, 16 mm, 18 mm, 20 mm |
| Material | Titanium Alloy |
| Surface Treatment | Micro-arc Oxidation |
| Qualification | CE / ISO13485 / NMPA |
| Package | Sterile Packaging 1pcs/package |
| MOQ | 1 Pcs |
| Supply Ability | 1000+ Pieces per Month |
Indicated for anterior interbody screw fixation from C2 to T1. The system is indicated for use in the temporary stabilization of the anterior spine during the development of cervical spinal fusions in patients with:
The system is indicated for temporary stabilization and anterior interbody screw fixation from C2 to T1 during spinal fusion, addressing degenerative disc disease, fractures/trauma, spinal deformities, tumors, pseudarthrosis, and revision of failed prior fusions.
The system is manufactured from high-grade titanium alloy with a micro-arc oxidation surface treatment, providing biocompatibility, excellent corrosion resistance, and high structural strength.
With an ultra-low profile thickness of only 1.9 mm and a seamless zero-profile interface between screw heads and the plate, it significantly lowers local anatomical impingement, protecting esophageal tissue and reducing the risk of postoperative dysphagia.
The system provides both Variable Angle Self-tapping Screws (diameters of Ф4.0 mm and Ф4.5 mm, lengths from 10 mm to 20 mm) and Variable Angle Self-drilling Screws (Ф4.0 mm, lengths from 10 mm to 20 mm).
The implants comply with international standards certified by CE, ISO13485, and NMPA. Each unit is delivered in sterile packaging (1 pcs/package) for immediate surgical readiness and complete traceability.