2TLQJ513
XC Medico
Anterior Cervical Approach
1 Pcs(72 Hours Delivery)
CE/ISO:9001/ISO13485.Etc
Titanium Alloy
integrated fixation 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).
Custom-Made 15 Days Delivery(Excluding Shipping Time)
FedEx. DHL.TNT.EMS.Etc
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An anterior cervical interbody cage with integrated fixation points, dual-mode compression options, ±15° multi-angle locking and radiopaque markers for selected cervical fusion procedures.
The XC Medico Cervical Titanium Cage-IV is a dedicated cervical interbody implant designed for selected anterior cervical discectomy and fusion procedures. Its integrated fixation architecture combines controlled compression, dual-mode planning options, multi-directional screw locking and radiopaque references in one cervical implant configuration.
The implant is available in four listed heights with a consistent 15.8 × 12.2 mm footprint. The supplied artwork identifies ±15° screw angulation and serrated endplate-contact surfaces; final size and fixation selection should follow 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.
Cage and screw fixation concept
5, 6, 7 and 8 mm
Listed footprint in millimeters
Listed multi-angle locking range
The high-strength titanium structure is designed to support resistance to compression, shear and subsidence-related loading in the intended application.
Serrated endplate-contact surfaces are designed to enhance grip and support stable cage positioning.
Integrated radiopaque markers are designed to support implant identification and position assessment under fluoroscopic imaging.
1. The integrated fixation design is intended to support resistance to rotation, shortening and shear while enabling controlled compression.
2. Controlled compression is designed to support accurate fixation planning while limiting unnecessary implant prominence.
3. The supplied artwork identifies dual fixation modes for flexible procedure planning and reconstruction needs.
4. Multi-directional locking provides a listed ±15° screw-angulation range for flexible fixation.
The integrated cage-and-screw architecture is designed to support rotational, shortening and shear stability with controlled compression.
The fixation architecture is designed to support controlled compression and accurate screw placement in the intended cervical application.
The supplied artwork identifies two fixation modes intended to support different procedure and reconstruction requirements.
Multi-directional screw locking provides a listed ±15° angulation range for flexible fixation planning.
| 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. Severe osteoporosis requires particular clinical assessment; patient selection, operative approach, fixation strategy and implant size depend on anatomy, bone quality, surgeon judgment and the approved technique.
The supplied artwork identifies a high-strength titanium alloy structure designed for rigidity and load-bearing performance.
Serrated endplate-contact geometry is designed to support cage positioning, while the hollow structure provides space for compatible graft material.
Integrated radiopaque markers support intraoperative visualization; final performance depends on correct selection, placement and the approved technique.
Confirm the exact screw size, trajectory and compatibility for the selected Cervical Titanium Cage-IV configuration.
A listed rongeur option for selected cervical decompression workflows.
A listed curette for selected cervical preparation workflows.
A listed forceps option for selected cervical decompression and preparation 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 artwork identifies integrated screw fixation, controlled compression, dual-mode planning options and ±15° multi-angle locking. Confirm the final approved configuration before ordering.
Integrated radiopaque markers support fluoroscopic position assessment, while serrated endplate-contact surfaces and integrated fixation are designed to support positional stability.
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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