Medicrea Launches Lifetime Warranty for Patient-Specific UNiD Constructs
Medicrea will implement a lifetime warranty on its patient-specific UNiDâ„¢ technology implanted in the U.S. from 11/1/16. Oct 26, 2016
Mobi-C the Most Widely Covered Intervertebral Prosthesis for Cervical Disc Replacement
Zimmer Biomet announced that its Mobi-C® Cervical Disc is now the most widely-covered device by U.S. commercial health insurers for 1- and 2-level cervical disc replacement.  Oct 26, 2016
Study Results: AMNIOX CLARIX Regenerative Matrix as Adjunct to Lumbar Discectomy
Results from a study of AMNIOX Medical’s proprietary cryopreserved Amniotic Membrane as an adjunct to lumbar discectomy indicate improved outcomes in disability scores at 6 weeks and 2 years. Oct 26, 2016
Spinal Elements and Mighty Oak Medical to Collaborate on FIREFLY Patient-Matched Surgery Solutions
Spinal Elements and Mighty Oak Medical will co-market the FIREFLY® surgical guidance system, comprising patient-matched bone models and intra-op pedicle screw guides created via 3D printing. Oct 26, 2016
First Surgeries with Medacta MySpine Low Profile Guide Following FDA Clearance
Medacta completed initial U.S. surgeries using its proprietary 3D-printed MySpine Patient Matched Technology Low Profile Guide, following FDA clearance. Oct 26, 2016
Ascential Product and Service Offering to Launch
Ascential is launching to offer an implant and delivery solution for lower acuity spinal procedures in ambulatory surgery center and hospital settings. Implants are manufactured by Stryker. Oct 25, 2016
Genesys Spine to Debut TiLock Cortical Spinal System
Genesys Spine is launching the TiLock Cortical Spinal System to provide an anatomy-conserving alternative to traditional pedicular fixation. Oct 25, 2016
Pinnacle Spine Launches InFill® V2 Lateral Interbody Device for Lumbar Spinal Fusion
Pinnacle Spine launched the InFill® V2 Lateral Interbody Device, featuring a large, single graft chamber and a large load-bearing surface area. Oct 25, 2016
Spineology Receives FDA Clearance of Rampart Duo Interbody Fusion System
Spineology received FDA 510(k) clearance to market the Rampart™ Duo™ Interbody Fusion System, reportedly the first device to combine PEEK, titanium and graft containment mesh elements. Oct 25, 2016
Early Outcomes with Porous PEEK COHERE Fusion Device
Vertera Spine announced initial successful outcomes using the COHERE® Cervical Interbody Fusion device. Oct 24, 2016
