Meditech Spine received FDA 510(k) clearance for CURE Lumbar Plating iView and QMax, with new sizing options to complement the company's existing CURE system.
Biologica Technologies is debuting initial clinical data from spinal applications using ProteiOS® growth factor. The product, which entered limited U.S. launch in 4Q17, is now available nationwide.
Medtronic gained FDA approval for use of Infuse bone graft with additional PEEK-based implants in oblique lateral and anterior lumbar interbody fusion procedures at one level.
DePuy Synthes commenced U.S. launch of PROTI 360°, interbody fusion systems featuring titanium-integrated PEEK with 360 degrees of titanium integration.Â
Episurf Medical entered into a distribution agreement in Hong Kong and established a U.S. subsidiary to conduct clinical studies for devices to treat localized cartilage injury.