XC Cervical Titanium Cage IV

Degenerative cervical disc disease is a primary clinical setting for this cage, used during anterior cervical discectomy and fusion, where a surgeon has selected titanium over PEEK for its direct bone-integration properties and this cage's larger footprint for the vertebral body anatomy involved in a given case. Procurement governance matters here as much as clinical fit: NHS spine units evaluating titanium cervical interbody options need this cage stocked reliably alongside matched anterior cervical plate components, which is where Medigear. Medigear UK's role as a stocking supplier matters to tender decisions and theatre list planning. uk's role as a stocking supplier matters to tender decisions and theatre list planning.

Larger vertebral body anatomy forms a second clinical setting, where this cage's 16.8mm by 13.8mm footprint may better suit the endplate dimensions involved than the smaller footprint confirmed on Cervical Titanium Cage-III. However, XC has not confirmed specific selection guidance, and this should be discussed with the surgical team.

Cervical myelopathy and radiculopathy represent a third clinical setting, where nerve root or spinal cord compression from degenerative or herniated disc material is addressed through discectomy, with this titanium cage restoring the resulting disc space and supporting fusion during recovery from the procedure and subsequent rehabilitation.

Revision anterior cervical surgery makes up a fourth clinical setting, where a surgeon may select a titanium cage as part of a revised construct, particularly where imaging suggests bone did not adequately integrate with a previous PEEK device at the operated level. 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.

Larger Footprint Than Cage-III Within the Same System

At 16.8mm by 13.8mm, this cage offers a larger footprint than Cervical Titanium Cage-III's 15.8mm by 12.2mm, while sharing the same height range and REF prefix, letting a surgical team match footprint to vertebral body size within one coordinated titanium system.

Direct Bone Integration Properties

General clinical literature reports that titanium can directly stimulate bone integration onto its surface, an advantage over PEEK, which functions as a spacer around which bone formation occurs rather than fusing to it directly.

Four Heights for Disc Space Restoration

Heights from 5mm to 8mm let a surgeon closely match the cage to the disc space measured on preoperative imaging.

Companion Product to Cervical Titanium Cage-III

Sharing a REF prefix and height range with Cage-III lets Medigear.uk supply both footprint sizes as a coordinated titanium cervical cage system from a single source.

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 Stand-Alone or Plate-Assisted Technique

The cage can generally be used either alone or alongside a separate anterior cervical plate, giving surgeons flexibility in construct design depending on the case.

REF-Coded Ordering for Simplified Procurement

Each height 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.

5mm Height (REF 2TLQJ513)

The shortest confirmed height, suited to smaller disc spaces.

6mm Height (REF 2TLQJ613)

A short-to-mid-range confirmed height.

7mm Height (REF 2TLQJ713)

A mid-to-larger confirmed height.

8mm Height (REF 2TLQJ813)

The tallest confirmed height, suited to larger disc spaces.

Fixed 16.8mm by 13.8mm Footprint

All four confirmed heights share the same footprint dimensions and differ only in height.

Titanium Construction

The cage is manufactured from titanium, offering direct bone integration properties distinct from XC's PEEK cage range.

REF-Coded Ordering System

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

Shared REF Prefix with Cervical Titanium Cage-III

Both references use the 2TLQJ prefix, distinguishing this titanium pair from the JQPEEK and JQ2PEEK prefixes used on XC's PEEK cage variants.

Larger Footprint Than Cage-III

At 16.8mm by 13.8mm, this footprint exceeds the 15.8mm by 12.2mm confirmed on Cage-III, while sharing the identical height range.

Compatible with Stand-Alone or Plate-Assisted Constructs

The cage generally supports use either alone or with a separate anterior cervical plate, depending on surgeon technique.

General Literature Reports Direct Bone Integration Advantage

Clinical literature generally reports that titanium's surface properties support a different fusion mechanism than PEEK's spacer function. However, specific outcome data for this XC reference has not been confirmed.

Completeness of the Table Not Confirmed

No natural terminal item on the source material signals whether the four confirmed heights represent the complete range for this reference.

The XC Cervical Titanium Cage-IV is a titanium interbody fusion device available in four heights (5mm to 8mm) with a fixed 16.8mm by 13.8mm footprint, under REF codes beginning 2TLQJ; it shares its REF prefix and height range with Cervical Titanium Cage-III while offering a larger footprint. It suits degenerative cervical disc disease, cases involving larger vertebral body anatomy, myelopathy and radiculopathy, and revision surgery, and may be used alongside XC's anterior cervical plate range, 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. However, check CE marking status and confirm whether heights beyond the four shown here exist with Medigear.uk before tender. Contact Medigear.uk for specifications, procurement assistance, or expert consultation.