Category: Lumbar Degenerative
The CONCORDE® Inline Lumbar Interbody System completes our CONCORDE Interbody cage platform for posterior MIS and open lumbar procedures. The system provides a posterior approach interbody fusion solution with a front to back lordotic cage option to address proper spinal alignment.
Made of a proprietary material of Carbon Fiber Reinforced Polymer, it has large areas for bone graft placement within the cage which allows the design to be a load-sharing device with 33% more bone graft area.1 This open architecture also provides for good graft to endplate surface contact.
The bulleted nose of the implant creates a self-distracting device that is designed to address collapsed disc spaces minimizing damage to endplates. With an option of a 5° front to back lordotic cage and shorter lengths the system is optimized for the PLIF procedure.
1.William DF, McNamara A, Turner RM. Potential of polyetheretherketone (PEEK) and carbon fiber-reinforced PEEK in medical applications. Journal of Material Science Letters (1987) 6:188-190.
The CONCORDE, CONCORDE Inline, CONCORDE Curve, COUGAR, DEVEX, and LEOPARD Systems are indicated for use as intervertebral body fusion devices in skeletally mature patients with degenerative disc disease (defined as discogenic back pain with degeneration of the disc confirmed by patient history and radiographic studies) at one or two contiguous levels of the lumbar spine (L2-S1). Patients should have six months of non-operative treatment prior to surgery. These implants are used to facilitate fusion in the lumbar spine and are placed via either a PLIF (CONCORDE, CONCORDE Inline), TLIF (CONCORDE, CONCORDE Inline, CONCORDE Curve, DEVEX, LEOPARD) or anterior (COUGAR) approach using autogenous bone. When used as interbody fusion devices these implants are intended for use with DePuy Spine supplemental internal fixation products.
The CONCORDE, CONCORDE Inline, CONCORDE Curve, COUGAR, DEVEX, and LEOPARD Systems are indicated for use in the thoracolumbar spine (i.e., T1-L5) to replace a diseased vertebral body resected or excised for the treatment of tumors, to achieve anterior decompression of the spinal cord and neural tissues, and to restore the height of a collapsed vertebral body. These systems are also indicated for treating fractures of the thoracic and lumbar spine. These systems are designed to restore the biomechanical integrity of the anterior, middle and posterior spinal column even in the absence of fusion for a prolonged period. When used as a vertebral body replacement device these systems are intended for use with DePuy Spine supplemental internal fixation products.
CONTRAINDICATIONS:1. Use of these systems is contraindicated when there is active systemic infection, infection localized to the site of the proposed implantation, or when the patient has demonstrated allergy or foreign body sensitivity to any of the implant materials.
WARNING: This product has labeling limitations. See package insert for additional warnings, precautions and possible adverse effects.
CAUTION: USA law restricts this device to sale by or on the order of physician.
|Bulleted nose cage||Allows access to collapsed spaces with minimal disruption of end plates|
|CFRP material||Creates a strong base material that allows for an open implant design|
|Robust size offering||Allows for varying patient anatomy|
|Lordotic trials||Allows for precise cage orientation and size measurement|
|Tantalum markers||Three markers allow for verification of placement and positioning|