Zimmer Biomet Launches Study of mymobility Apple Watch App Joint Replacement ORTHOFLASH Zimmer Biomet launched a clinical study of mymobility, an Apple Watch app to support connection between hip and knee replacement patients and their surgical care teams. Oct 15, 2018
Field Orthopaedics Launching Micro Screw in EMEA Region ORTHOFLASH Trauma Field Orthopaedics will enter the EMEA region with launch of its Micro Screw system. Oct 15, 2018
X-Bolt Orthopaedics Gains FDA Clearance for Hip Nailing and Hip Plating ORTHOFLASH Trauma X-Bolt Orthopaedics achieved FDA 510(k) clearance for X-Bolt Hip Nailing and Hip Plating fixation. Oct 15, 2018
Medacta Gains FDA Clearance, Announces First U.S. Procedure for Hip Implants Joint Replacement ORTHOFLASH Medacta received FDA 510(k) clearance to market its Mpact 3D Metal and Augments 3D Metal implants for use in total and revision hip arthroplasty. Oct 11, 2018
Arthrosurface Launches OVOMotion Stemless Total Shoulder Joint Replacement ORTHOFLASH Arthrosurface commenced U.S. launch of the OVOMotion stemless shoulder arthroplasty system. Oct 11, 2018
Catalyst OrthoScience Launches 3-Peg Glenoid Implant Joint Replacement ORTHOFLASH Catalyst OrthoScience commenced launch of its 3-Peg Glenoid implant, to be used with the CSR total shoulder. Oct 11, 2018
K2M Expands MESA Platform with FDA Clearance for Sagittal Imbalance Application ORTHOFLASH Spine K2M received additional FDA 510(k) clearance for the MESA® Spinal System, supporting use of sagittal plane correction in idiopathic scoliosis. Oct 11, 2018
SeaSpine Prices $50MM Public Offering of Stock Investments The Numbers SeaSpine closed its underwritten public offering of 3,250,000 shares of its common stock for US $15.50/share, for gross proceeds of ~$50.4MM. Oct 11, 2018
Episurf Medical Granted Additional Patent in China Joint Replacement ORTHOFLASH Episurf Medical was granted a new patent in China covering the drill guide for the Episealer® Femoral Twin implant. Oct 10, 2018
SpineEX Gains FDA Clearance for Sagittae LLIF ORTHOFLASH Spine SpineEX received FDA 510(k) clearance to market its Sagittae® expandable device for minimally invasive lateral lumbar interbody fusion. Oct 10, 2018