LDR is now Zimmer Biomet

Product Overview

The Avenue® L Lateral Lumbar Cage is designed for strength, versatility, and stability. It represents the pinnacle of lateral lumbar cage evolution incorporating zero-profile, intradiscal, and integrated fixation. The enhanced in-line, self-guided VerteBRIDGE® Plating Technology facilitates simplified cage insertion all through a direct, minimally invasive approach.

Features

Features

  • Comprehensive offering of footprints to meet different patient anatomy and provide for optimal endplate contact
  • Beveled nose to ease insertion
  • I-beam design to increase the rigidity of the cage and support the graft during insertion into the intervertebral space
  • Intra-operative adjustment of the Cage Holder to ensure optimal positioning of the cage prior to insertion of VerteBRIDGE plating
  • Guided in-line plate delivery
  • Sterile packaging for assured product quality and absolute traceability

VerteBRIDGE® Plating Technology

  • Zero-profile design with no hardware protruding outside of the vertebral bodies
  • Self-locking plates designed for initial and long-term stability
  • Self-guided, curved plates ease insertion
  • Inserter provides protection of anatomic structures during plate placement
  • Innovative plate delivery system optimized for the direct lateral approach

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Surgical Technique

Indications for Use (IFU)

The Avenue® L Interbody Fusion System is indicated for intervertebral body fusion of the lumbar spine, from L2 to S1, in skeletally mature patients who have had six months of non-operative treatment. The device is intended for use at either one level or two contiguous levels for the treatment of degenerative disc disease (DDD) with up to Grade I spondylolisthesis. DDD is defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies. The device system is designed for use with or without integrated fixation and must be used in conjunction with posterior supplemental fixation (e.g., pedicle screws). The device system is intended to be used with autograft to facilitate fusion.