Lumbar Facet Disease Clinical Trial
Official title:
A Post-Market Study of Transfacet Lumbar Spine Fixation and Fusion Utilizing the PERPOS™ PLS System
The purpose of this study is to utilize the PERPOS™ PLS System for transfacet lumbar spine fixation to evaluate its effect on patients' level of pain, procedural complications and functional status.
The PERPOS™ PLS System involves a minimally invasive, percutaneous implant procedure via a
small incision.
The PERPOS™ PLS is intended for lumbar bilateral facet fixation, with or without bone graft,
at single or multiple levels from L1 to S1.
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Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment