July 14, 2015 | By Lilian
German company Joimax, a developer of technology used in minimally invasive endoscopic spinal surgeries, said it received 510(k) clearance from the U.S. Food and Drug Administration to market its EndoLIF On-Cage 3D printed titanium implant.
Joimax said its EndoLIF On-Cage implant, produced with Electron Beam Melt (EBM) technology, allows surgeons to utilize an inter-muscular approach, similar to a mini transforaminal lumbar interbody fusion (TLIF), into the intervertebral disc, enabling endoscopic-assisted fusion. The cage displays a porous surface with diamond cell structure, providing an optimal base for cell proliferation and bone growth. Two large openings, which may be filled with autogenous bone, support the creation of a straight column for fusion.
Dr. Ralf Wagner, LIGAMENTA Spine Center, Frankfurt and Dr. Bernd Illerhaus, ONZ, Datteln/Recklinghausen, two German spine specialists, have already performed more than 200 out of 600 EndoLIF procedures in Europe. "The access is dura and nerve-gentle, preserves the dorsal bony structures and we can avoid scar tissue because of the stepwise tissue dilation," said Dr. Illerhaus.
"With the EndoLIF program, joimax offers a complete endoscopic-assisted solution for spinal stabilization and fusion. In the future, we will be able to treat patients with even more gentle techniques," comments Wolfgang Ries, CEO and founder of joimax. "Our next development will be an EndoLIF Cage on the basis of our iLESSYS Delta system for posterior lumbar inter-body fusion (PLIF)."
Founded in Karlsruhe, Germany, in 2001, joimax is one of the leading medical device companies in minimally invasive spinal surgery. The company, which opened its Irvine subsidiary in 2005, said it is active in 40 countries and its methods have been successfully used in roughly 150,000 surgeries.
Posted in 3D Printing Applications
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