Idys™-PTLIF cage has been designed by a team experienced in the development of spinal instrumentation. Made of PEEK-OPTIMA, Idys™-PTLIF cages are specially designed for posterior lumbar and lumbo-sacral intersomatic arthrodesis. Idys™–PTLIF allows surgical approaches: - Unilateral posterior approach (TLIF-Oblique) - Bilateral posterior approach (PLIF) The design team focused on creating a PTLIF cage adapted to vertebral anatomy that would maintain disc height, restore lumbar lordosis and stabilize the treated segment, thus creating optimal conditions for bone fusion. This instrumentation is also versatile and can be used with Idys™-PTLIF surgical technique.

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Indications for use

The Idys™ LIF Cages are indicated for use with autogenous bone graft in patients with degenerative disc disease (DDD) at one or two levels from L2 to S1. These DDD patients may also have up to Grade 1 Spondylolisthesis or retrolisthesis at the involved levels. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should be skeletally mature and have had six months of non-operative treatment. These implants may be implanted via a posterior and/or transforaminal approach. These devices are intended to be used with supplemental fixation instrumentation which has been cleared by the FDA for use in the lumbar spine.

Federal law (USA) restricts this device to sale by or on the order of a physician. Prior to using any Clariance device, please review the instructions for use and surgical technique for a complete listing of indications, contraindications, warnings, precautions, potential adverse events, and directions for use.

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