CAUTION – Investigational device. Limited by Federal (or United States) law to investigational use.
This proof-of-concept study is sponsored by SynerFuse, Inc., and is conducted under an approved IDE (G1900454) from FDA. Safety and efficacy for this indication have not been established.
Feasibility Study Completed
15 fusion patients
Sites: Minneapolis, Minnesota and South Bend, Indiana.
SynerFuse® has partnered with RQM+ for clinical trial monitoring and regulatory services. We are confident that together we can reduce chronic back pain and improve patient quality of life.
Patient Stories
Michael’s Story
Thanks to the groundbreaking SynerFuse™ e-TLIF™ procedure, Michael Jonatzke is up and moving around pain free, from long daily walks with his two dogs to now sleeping in his bed.
Jason’s Story
"It's changed my quality of life. I can get down [to] the ground and play with my grandkids and chase them around now. I feel like a little kid." – Jason Fleck, post SynerFuse™ e-TLIF™ procedure.
Sara’s Story
Sara Grieser struggled with back pain for over a decade before the SynerFuse™ e-TLIF™ procedure. Now virtually pain-free, she can sit comfortably through her children’s sports games and performances.
Dawn’s Story
Dawn Rootes-Husted describes the SynerFuse™ e-TLIF™ procedure as a "game changer" and says, "I love riding my motorcycle, and that is something that I've gotten back into again.”
