ProCoral ADR Cervical Disc Prosthesis
Non-sterile cervical disc prosthesis designed to preserve motion following cervical disc replacement.
- Product type
- Motion Preservation
- Application
- Anterior cervical disc arthroplasty, C3–C7
- Brand / Manufacturer
- Prodorth / RD Medikal
- Regulatory
- TFDA No. 037314
ProCoral ADR Cervical Disc Prosthesis
ProCoral is a long-term cervical disc prosthesis composed of two independent titanium-alloy endplates connected by a PEEK pin and support structure. The design is intended to preserve relative cervical motion, including axial rotation, flexion-extension and lateral bending, rather than create a fused motion segment.
Motion-preservation design
Axial rotation
Flexion-extension
Lateral bending
Anterior cervical implantation using dedicated instrumentation
Models & specifications
Configurations shown here are a website summary. Use the current approved product documentation for final model selection and procedural details.
| Footprint: Depth × Length (mm) | Available heights (mm) | Model family |
|---|---|---|
| 12 × 14 | 5.0–8.5 in 0.5 mm increments | 102.08 0250–0285 |
| 14 × 14 | 5.0–8.5 in 0.5 mm increments | 102.08 0150–0185 |
| 14 × 16 | 5.0–8.5 in 0.5 mm increments | 102.08 0050–0085 |
Supplied non-sterile. The approved IFU requires cleaning and decontamination before sterilization and recommends steam sterilization in an autoclave at 134°C for 18 minutes before surgical use. Store carefully at room temperature.
Indications overview
The points below summarize the product family. Final patient selection and clinical use must follow the applicable approved labeling and Instructions for Use.
Skeletally mature patients requiring reconstruction at C3–C7
Degenerative disc disease
Cervical disc herniation
Marked reduction in disc height
Facet-joint degeneration such as osteophyte-related disease, as described in the approved IFU
ProCoral ADR Cervical Disc Prosthesis
Product imagery is provided for portfolio identification. Model-specific components, dimensions and technique should be confirmed against current approved documentation.
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