There are over 90 peer-reviewed publications on the coflex device, making it one of the most studied lumbar spinal devices on the market.
coflex is the FIRST AND ONLY lumbar spinal device with Level I evidence in two separate clinical studies, against the two standard treatments (decompression alone and fusion), across two different countries.
Both studies prove coflex relieves significant leg and back pain, maintains motion at both index and adjacent levels, decreases compensatory pain management, increases physical function, and extends the durability and sustainability of a decompression procedure.
This makes coflex is the exclusive posterior lumbar motion preservation solution with proven long-term outcomes for durable pain relief and stability.
Next: U.S. FDA Trial Overview