FDA Clears Binder Biomedical’s LOGIC Spinal Fusion Device

The U.S. FDA recently approved Binder Biomedical’s LOGIC standalone intervertebral body fusion device for treatment of degenerative disc disease.

Advertisement

The LOGIC system was crafted for use in direct anterior surgical approach of the lumbar spine. The national launch will take place in the fourth quarter of 2014.

The device is made out of PEEK-OPTIMA, the proprietary polymer from Invibio Biomaterial Solutions.

More Articles on Devices:
Spine Wave Implements iTraycer for Implants
X-Stop Spine Surgery: Outcomes Analysis   
Lanx Hosts Lateral Interbody Fusion & Fixation System Demonstration

At the Becker’s 32nd Annual Meeting: The Business and Operations of ASCs, taking place October 29-31 in Chicago, ASC leaders, surgeons and healthcare executives will explore strategies to drive growth, enhance operational performance, navigate reimbursement challenges and prepare for the future of ambulatory surgery. Apply for complimentary registration now.

Register to Attend Webinar

160 ambulatory leaders just ranked the EHR as the single system most overdue for AI reinvention

Tuesday, August 11
12:00 PM - 1:00 PM CDT

Presenter: Gautam Shah, MBA, FACHDM, NextGen Healthcare

Advertisement

Next Up in Spinal Tech

Advertisement

Comments are closed.