2TLQJ512
XC Medico
Anterior Cervical Approach
1 Pcs(72 Hours Delivery)
CE/ISO:9001/ISO13485.Etc
Titanium Alloy
radiopaque cervical cage
Laser marking, custom anodizing colors & packaging.
Free surgical videos, user manuals & technical guidance.
30-day hassle-free returns (for unused items in original packaging).
18 Months (Instruments) | 24 Months (Power Tools) | 36 Months (Implants).
FedEx. DHL.TNT.EMS.Etc
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A titanium anterior cervical interbody cage with radiopaque markers, serrated endplate-contact surfaces and a hollow graft chamber for selected cervical fusion procedures.
The XC Medico Cervical Titanium Cage-III is a dedicated cervical interbody implant designed for selected anterior cervical discectomy and fusion procedures. Its titanium structure combines a radiopaque profile, serrated endplate-contact surfaces and a central chamber for placement of compatible graft material.
The implant is available in four listed heights with a consistent 15.8 × 12.2 mm footprint. Final size selection should follow patient anatomy, endplate preparation, surgical planning and the approved technique.
For broader planning, distributors can review the XC Medico ACDF surgical solution, interbody cage portfolio and spine implant range.
Listed titanium alloy
5, 6, 7 and 8 mm
Listed footprint in millimeters
Integrated radiopaque reference
The TC4 titanium structure is designed to provide mechanical support under the intended cervical interbody loading conditions.
Integrated radiopaque markers are designed to support cage identification and position assessment under fluoroscopic imaging.
The supplied product material identifies TC4 titanium alloy for the cervical interbody implant.
1. Integrated radiopaque markers support fluoroscopic visualization and position assessment.
2. TC4 titanium construction is designed for compressive and shear loading in the intended application.
3. Serrated endplate-contact surfaces are designed to enhance grip at the prepared interface.
4. The hollow central chamber provides space for compatible bone-graft material.
The supplied artwork describes the cage elastic modulus as higher than bone.
The titanium structure is intended to provide mechanical support within the selected cervical interbody space.
Surface serrations are designed to enhance grip and support positional stability after placement.
The open central structure provides space for placement of compatible graft material according to the surgical plan.
| Configuration | Product Dimensions | Listed Height |
|---|---|---|
| Configuration 1 | 5 × 15.8 × 12.2 mm | 5 mm |
| Configuration 2 | 6 × 15.8 × 12.2 mm | 6 mm |
| Configuration 3 | 7 × 15.8 × 12.2 mm | 7 mm |
| Configuration 4 | 8 × 15.8 × 12.2 mm | 8 mm |
Confirm the dimension order, available inventory and final product code with the current approved specification before ordering.
These application areas reflect the supplied product artwork. Patient selection, operative approach and implant size depend on clinical assessment, anatomy, surgeon judgment and the approved technique.
The source material identifies imported TC4 titanium alloy for mechanical performance and implant material compatibility.
The listed manufacturing route includes CNC machining, wire EDM, anodizing, electropolishing and surface finishing.
The supplied artwork states that mechanical test records are archived for more than three years and lists a quality rate of at least 98.9%.
Confirm the exact screw system and compatibility for the selected procedure.
A listed retraction instrument for the procedure-matched workflow.
A listed preparation instrument for selected cervical procedures.
A listed instrument option for selected decompression workflows.
Additional system planning may include an anterior cervical plate, the anterior cervical plate instrument set or the dedicated cervical cage instrument set. Product compatibility must be confirmed before ordering; these links are provided for workflow navigation, not as automatic compatibility claims.
Use this space to present the cage structure, size range, radiopaque markers, serrated surfaces and graft chamber. Product video content should not replace the approved surgical technique.
Share the following information for implant, instrument and documentation review.
| Matching Item | Information to Provide | Purpose |
|---|---|---|
| Procedure / Cervical Level | Planned procedure and treated level | Application review |
| Cage Size | Required height and footprint confirmation | Size matching |
| Matching System | Plate, screws and instrument requirements | Workflow review |
| Supply Details | Quantity, packaging, target country and documents | Quotation and market review |
Send the intended procedure, cervical level, required cage height, quantity, matching instrument needs and target market for product matching and quotation.
Request Product Matching Request Spine CatalogIt is designed as an anterior cervical interbody implant for selected cervical fusion procedures, including planned ACDF workflows.
The supplied product table lists 5 × 15.8 × 12.2 mm, 6 × 15.8 × 12.2 mm, 7 × 15.8 × 12.2 mm and 8 × 15.8 × 12.2 mm configurations.
The supplied product artwork identifies TC4 titanium alloy. Confirm the current approved material specification for the target market before ordering.
Integrated radiopaque markers are designed to support fluoroscopic position assessment, while the hollow central chamber provides space for compatible graft material.
No. It supports product identification and distributor matching only. Final selection and use should follow the approved technique, surgeon judgment and applicable requirements.
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