XC Titanium Mesh Cage

Cervical spondylotic myelopathy and related degenerative conditions are a primary clinical setting for this cage, used following anterior cervical corpectomy to reconstruct the anterior column and support spinal cord decompression at the affected level of the cervical spine. Procurement governance matters here as much as clinical fit: NHS spine units evaluating corpectomy reconstruction options need this cage stocked reliably across the confirmed diameter range and length, which is where Medigear.uk's role as a stocking supplier matters to tender decisions and theatre list planning.

Spinal tumour resection is a second important clinical setting, where general clinical literature documents titanium mesh cages as a long-established reconstruction option following vertebral body removal for tumour, alongside newer alternatives such as three-dimensional printed artificial vertebral bodies that some recent literature has compared directly against this device category.

Trauma and significant vertebral fracture represent a third important clinical setting, where a corpectomy may be required following severe vertebral body fracture, with this cage providing anterior column support during the fusion and healing process across cervical, thoracic, or lumbar levels of the spine as needed.

Spinal infection is a fourth and equally important clinical setting, where corpectomy and reconstruction may be required to remove infected bone and restore structural support to the affected segment of the spine. Medigear.uk supports single or small-quantity ordering of this cage alongside the larger bulk distributor accounts it also serves, so a specialist clinic is not required to commit to trust-scale volumes to access it for a single reconstruction case.

Established Device Category with Decades of Published Literature

Titanium mesh cages are a long-established device category in spine surgery, with extensive peer-reviewed literature documenting outcomes across cervical, thoracic, and lumbar corpectomy reconstruction.

Six Diameters for Anatomical Fit Across Spinal Levels

Diameters from 10mm to 20mm let a surgeon select a cage suited to the vertebral body footprint involved, spanning the range typically needed from cervical through to lumbar reconstruction.

Cut-to-Length Stock Design for Intraoperative Flexibility

The confirmed 100mm stock length is designed to be cut to the exact defect dimension intraoperatively, letting a single stock item serve a range of defect sizes.

Open Mesh Structure for Bone Graft Integration

General literature describes the mesh design as supporting bone graft packing and subsequent bone growth through the structure, a mechanism generally associated with promoting fusion.

ISO 13485-Certified Manufacturing for Procurement Governance

XC's quality management system is certified to ISO 13485 at company level, giving hospital procurement teams and distributors a documented baseline to evaluate against tender requirements. Buyers should confirm CE marking status for this specific reference before submitting to formal procurement processes.

Compatible with Anterior Plate Systems

Titanium mesh cages of this kind are frequently combined with a separate anterior plate for additional stability, letting Medigear.uk supply a coordinated construct alongside the plate systems already covered elsewhere in this catalogue.

REF-Coded Ordering for Simplified Procurement

Each diameter is ordered under its own REF code, giving procurement teams a clear, unambiguous way to specify the exact cage needed against a surgeon's preoperative plan.

Small-Batch Ordering for Specialist Clinics and Independent Practices

Independent spine surgeons and smaller private surgical centres do not always need trust-scale order volumes, and Medigear.uk supports single or small-quantity purchasing of this cage alongside its larger distributor accounts.

10mm Diameter

The smallest confirmed diameter, suited to smaller vertebral body footprints, typically cervical level.

12mm and 14mm Diameters

Mid-range confirmed diameters spanning a common cervical and smaller thoracolumbar reconstruction range.

16mm and 18mm Diameters

Larger confirmed diameters suited to thoracolumbar vertebral body footprints.

20mm Diameter

The largest confirmed diameter, suited to larger lumbar vertebral body footprints.

100mm Stock Length

Confirmed across all six diameters, designed to be cut to the required intraoperative length.

Titanium Construction

The cage is manufactured from titanium, consistent with the biocompatibility and radiopacity generally associated with this device category in clinical literature.

REF-Coded Ordering System

Each diameter has its own REF code, providing a clear, unambiguous way to specify the exact cage needed for a given order.

Open Mesh Design

Supports bone graft packing and bone growth through the mesh structure, consistent with general titanium mesh cage design.

Distinct Product Category from XC's Interbody Cages

Used for vertebral body replacement following corpectomy rather than standard disc-space interbody fusion, a genuinely different clinical application from the PLIF, TLIF, and cervical cages covered elsewhere in this catalogue.

Spans Cervical Through Lumbar Diameter Range

The confirmed 10mm to 20mm range covers the diameters generally needed across cervical, thoracic, and lumbar corpectomy reconstruction.

Subsidence Considerations Documented in General Literature

General clinical literature identifies subsidence as a recognised complication of this device category, with reported rates varying across published series; this provides information relevant to preoperative planning and patient counselling.

Compatible with Anterior Plate Systems

Generally used in combination with a separate anterior plate for additional construct stability, consistent with plate systems already covered elsewhere in this catalogue.

The XC Titanium Mesh Cage is a titanium vertebral body replacement device confirmed across six diameters (10mm to 20mm) at a 100mm stock length, under REF codes beginning with TI, for spinal reconstruction following corpectomy. It is a genuinely different product category from XC's interbody cages covered elsewhere in this catalogue, addressing cervical spondylotic myelopathy, spinal tumour resection, trauma, and spinal infection, from primary hospital theatre work through to smaller private surgical centres. XC's ISO 13485-certified manufacturing gives procurement teams a documented baseline for evaluation, and extensive general clinical literature broadly supports the titanium mesh cage category. However, confirm CE marking status and outcome data specific to this exact XC reference with Medigear.uk before tender. Contact Medigear.uk for specifications, procurement assistance, or expert consultation.