PD-31-203: Providence Medical CAVUX Cervical Cage-X Lordotic Titanium Interbody Spacer for ACDF, 4mm

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Providence Medical CAVUX Cervical Cage-X – Lordotic Titanium Interbody Spacer with Enhanced Graft Access

The CAVUX® Cervical Cage-X by Providence Medical Technology is a 4mm titanium interbody fusion device engineered for single-level ACDF procedures (C3–C7). Compared to the Cage-B, the Cage-X features a lordotic profileto help restore cervical sagittal alignment and a larger graft window designed to increase fusion surface area and improve visualization during placement. Like all CAVUX implants, it is pre-mounted on a sterile, disposable inserter to streamline the surgical workflow. The Cage-X maintains a similar tapered nose for smooth insertion but offers biomechanical advantages in cases where lordosis restoration is desired.

Product Code: PD-31-203

• Material: Titanium alloy (Ti-6Al-4V ELI)
• Implant Profile: Lordotic
• Height: 4mm
• Indications: Single-level ACDF (C3–C7)
• Graft Window: Enlarged cavity for improved visualization and fusion potential
• Inserter: Pre-mounted on sterile, single-use delivery instrument
• MRI Compatibility: MR Unsafe
• Implantable

Contents

• One CAVUX Cervical Cage-X titanium implant
• Disposable sterile insertion tool

Features

• Lordotic design supports sagittal alignment
• Expanded graft window for enhanced bone integration
• Roughened surface promotes ongrowth
• Tapered leading edge aids in controlled insertion

Sterilization

• Device Packaged as Sterile: Yes
• Requires Sterilization Prior to Use: No
• Single-Use, Disposable

Additional Details

• Brand: Providence Medical Technology
• Category: Spinal Implants
• Type: Cervical Interbody Fusion Device
• FDA Product Code: ODP
• FDA Product Code Name: Intervertebral Fusion Device with Bone Graft, Cervical
• GMDN Term Code: 38161
• GMDN Term Name: Metallic spinal interbody fusion cage
• GMDN Term Definition: A device intended to be implanted into the space of an intervertebral disc that has been partially or totally removed during surgery in order to allow bone fusion between two contiguous vertebral bodies, typically in the treatment of degenerative disc disease (DDD). It is in the form of a hollow, porous, threaded and/or fenestrated cylindrical or geometrical device made of metal [e.g., titanium (Ti)] that provides mechanical stability and sufficient space for therapeutic spinal bone fusion to occur; bone graft is typically used to help with osseointegration. Fixation screws and devices associated with implantation may be included with the device.

Providence Medical Technology specializes in innovative solutions for cervical spine disorders, with a focus on minimally invasive, posterior approaches. Their CORUS™ Spinal System is a key component of their PACS™ (Posterior Cervical Stabilization) platform, offering a comprehensive set of implants and instruments for posterior cervical fusion. Designed to treat conditions like cervical radiculopathy and myelopathy, the CORUS system enables tissue-sparing procedures that promote stability and fusion with reduced surgical disruption. Combined with their proprietary DTRAX® implants, Providence delivers a streamlined, patient-focused approach to cervical spine care.