Keylink Composite Intervertebral Cage
Composite lumbar intervertebral cage combining PEEK and titanium-alloy technologies.
- Product type
- Lumbar Interbody Fusion
- Application
- Lumbar Interbody Fusion
- Manufacturer / Brand
- Socko Medical Co., Ltd.
- Regulatory
- TFDA No. 008436
Keylink Composite Intervertebral Cage
A composite lumbar interbody cage designed for L1-S1 fusion applications. The platform combines PEEK and titanium-alloy components in a single interbody construct.
Composite PEEK/titanium design
Lumbar interbody application
Multiple heights and lengths
Dedicated instrumentation
Models & specifications
Configurations shown here are a website summary. Use the current approved product documentation for final model selection and procedural details.
Multiple model families
Lengths include 26, 28, 30 and 32 mm in the approved model tables
Multiple height options
Gamma sterilized. The approved labeling specifies a 5-year shelf life.
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.
L1-S1 levels
Lumbar degenerative disc disease
Pseudarthrosis or failed spinal fusion
Revision following disc-removal surgery
Degenerative spondylolisthesis and Grade I spondylolisthesis
Keylink Composite Intervertebral Cage
Product imagery is provided for portfolio identification. Model-specific components, dimensions and technique should be confirmed against current approved documentation.
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