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11101 NEULLEN laminoplasty Plate
| Product No. | Height |
| 11101012 | 12 |
| 11101014 | 14 |
| 11101016 | 16 |
10511 NEULLEN screws (cross self-tapping)
| Product No. | Dia | Length |
| 11101012 | 2.5 | 6 |
| 11101014 | 8 | |
| 11101016 | 10 |
10511 NEULLEN screws (cross self-tapping and self-drilling)
| Product No. | Dia | Length |
| 11101012 | 2.5 | 6 |
| 11101014 | 8 | |
| 11101016 | 10 |
Pre-contoured to match the cervical spine’s natural curvature.
Reduces intraoperative plate bending.
Enhances surgical efficiency and accuracy.
Multiple sizes and adjustable slots for optimal fit across patient anatomies.
Helps maintain proper laminar opening during the healing process.
Low-profile screw heads reduce risk of soft tissue irritation.
Secure screw-plate locking mechanisms to prevent backing out.
Multiple locking options (e.g., self-tapping, variable angle).
Made from biocompatible titanium alloy (Ti-6Al-4V).
High strength-to-weight ratio and excellent corrosion resistance.
Radiolucent under imaging for easy postoperative evaluation.
Facilitates controlled laminar opening.
Maintains spinal canal decompression effectively.
Supports hinge preservation technique for bone healing.
Ergonomic and intuitive instrumentation.
Designed to reduce operative time and improve reproducibility.
Includes plate benders, drill guides, depth gauges, and screwdrivers.
Slim profile minimizes soft tissue disruption.
Reduces post-operative pain and muscle trauma.
Fixed and variable angle screws available.
Screw lengths and diameters optimized for cervical lamina and lateral mass fixation.
NEULEN Cervical Laminoplasty System – Indications for Use
The NEULEN Cervical Laminoplasty System is intended for use in posterior cervical spine surgery to provide stabilization and support during the healing process following decompression procedures. Specifically, it is indicated for:
✅ Laminoplasty Procedures
Reconstruction and stabilization of the cervical lamina following open-door or double-door laminoplasty techniques.
✅ Cervical Spinal Canal Stenosis
To relieve pressure on the spinal cord due to congenital or acquired spinal canal narrowing (e.g., ossification of the posterior longitudinal ligament (OPLL), spondylosis).
✅ Multilevel Cervical Myelopathy
When multiple cervical segments require decompression to alleviate spinal cord compression symptoms.
✅ Degenerative Cervical Spine Disorders
Such as cervical spondylotic myelopathy (CSM), where non-fusion techniques like laminoplasty are preferred.
Patient Selection Criteria
The system is typically used in adult patients:
With preserved cervical alignment.
Without significant cervical instability.
Who require spinal cord decompression without fusion.

The NEULEN system is used in posterior cervical spine surgeries to stabilize the lamina during laminoplasty procedures. It supports spinal decompression in patients with conditions such as cervical myelopathy, spinal stenosis, and ossification of the posterior longitudinal ligament (OPLL).
It is compatible with both open-door and double-door laminoplasty techniques. The system is designed to facilitate controlled laminar opening while maintaining alignment and stability.
The system components are manufactured from medical-grade titanium alloy (Ti-6Al-4V), which offers excellent strength, biocompatibility, and radiographic clarity.
Yes. NEULEN plates are anatomically pre-contoured to match the natural curvature of the cervical spine, reducing the need for intraoperative bending and improving fit and performance.
Yes. The system offers both fixed-angle and variable-angle screw options to provide surgical flexibility and optimal fixation based on patient anatomy.
NEULEN provides a range of self-tapping screw lengths and diameters, specifically optimized for lateral mass and laminar fixation in the cervical spine.
Yes. The plates and screws are low-profile to reduce the risk of soft tissue irritation and minimize postoperative discomfort.
Yes. The system allows for the use of bone spacers or bone grafts at the open hinge site to promote fusion and structural support.
Being made of titanium, the system is MRI- and CT-compatible, allowing for clear postoperative imaging with minimal artifact.
The system includes a comprehensive set of ergonomic instruments, such as:
Plate holders and benders
Drill guides
Depth gauges
Torque-limiting screwdrivers
11101 NEULLEN laminoplasty Plate
| Product No. | Height |
| 11101012 | 12 |
| 11101014 | 14 |
| 11101016 | 16 |
10511 NEULLEN screws (cross self-tapping)
| Product No. | Dia | Length |
| 11101012 | 2.5 | 6 |
| 11101014 | 8 | |
| 11101016 | 10 |
10511 NEULLEN screws (cross self-tapping and self-drilling)
| Product No. | Dia | Length |
| 11101012 | 2.5 | 6 |
| 11101014 | 8 | |
| 11101016 | 10 |
Pre-contoured to match the cervical spine’s natural curvature.
Reduces intraoperative plate bending.
Enhances surgical efficiency and accuracy.
Multiple sizes and adjustable slots for optimal fit across patient anatomies.
Helps maintain proper laminar opening during the healing process.
Low-profile screw heads reduce risk of soft tissue irritation.
Secure screw-plate locking mechanisms to prevent backing out.
Multiple locking options (e.g., self-tapping, variable angle).
Made from biocompatible titanium alloy (Ti-6Al-4V).
High strength-to-weight ratio and excellent corrosion resistance.
Radiolucent under imaging for easy postoperative evaluation.
Facilitates controlled laminar opening.
Maintains spinal canal decompression effectively.
Supports hinge preservation technique for bone healing.
Ergonomic and intuitive instrumentation.
Designed to reduce operative time and improve reproducibility.
Includes plate benders, drill guides, depth gauges, and screwdrivers.
Slim profile minimizes soft tissue disruption.
Reduces post-operative pain and muscle trauma.
Fixed and variable angle screws available.
Screw lengths and diameters optimized for cervical lamina and lateral mass fixation.
NEULEN Cervical Laminoplasty System – Indications for Use
The NEULEN Cervical Laminoplasty System is intended for use in posterior cervical spine surgery to provide stabilization and support during the healing process following decompression procedures. Specifically, it is indicated for:
✅ Laminoplasty Procedures
Reconstruction and stabilization of the cervical lamina following open-door or double-door laminoplasty techniques.
✅ Cervical Spinal Canal Stenosis
To relieve pressure on the spinal cord due to congenital or acquired spinal canal narrowing (e.g., ossification of the posterior longitudinal ligament (OPLL), spondylosis).
✅ Multilevel Cervical Myelopathy
When multiple cervical segments require decompression to alleviate spinal cord compression symptoms.
✅ Degenerative Cervical Spine Disorders
Such as cervical spondylotic myelopathy (CSM), where non-fusion techniques like laminoplasty are preferred.
Patient Selection Criteria
The system is typically used in adult patients:
With preserved cervical alignment.
Without significant cervical instability.
Who require spinal cord decompression without fusion.

The NEULEN system is used in posterior cervical spine surgeries to stabilize the lamina during laminoplasty procedures. It supports spinal decompression in patients with conditions such as cervical myelopathy, spinal stenosis, and ossification of the posterior longitudinal ligament (OPLL).
It is compatible with both open-door and double-door laminoplasty techniques. The system is designed to facilitate controlled laminar opening while maintaining alignment and stability.
The system components are manufactured from medical-grade titanium alloy (Ti-6Al-4V), which offers excellent strength, biocompatibility, and radiographic clarity.
Yes. NEULEN plates are anatomically pre-contoured to match the natural curvature of the cervical spine, reducing the need for intraoperative bending and improving fit and performance.
Yes. The system offers both fixed-angle and variable-angle screw options to provide surgical flexibility and optimal fixation based on patient anatomy.
NEULEN provides a range of self-tapping screw lengths and diameters, specifically optimized for lateral mass and laminar fixation in the cervical spine.
Yes. The plates and screws are low-profile to reduce the risk of soft tissue irritation and minimize postoperative discomfort.
Yes. The system allows for the use of bone spacers or bone grafts at the open hinge site to promote fusion and structural support.
Being made of titanium, the system is MRI- and CT-compatible, allowing for clear postoperative imaging with minimal artifact.
The system includes a comprehensive set of ergonomic instruments, such as:
Plate holders and benders
Drill guides
Depth gauges
Torque-limiting screwdrivers