Extremity Medical Receives FDA 510(k) Clearance for Axis Charcot Fixation
Extremity Medical announced FDA 510(k) clearance of the Axis Charcot fixation system. Jul 14, 2017
CTL Medical to Market G-21 Products in US
CTL Medical entered into an agreement to market G-21’s bone cement, kyphoplasty and vertebroplasty products in the U.S. Jul 13, 2017
Tyber Medical Receives FDA 510(k) Clearance for TyFix
Tyber Medical received FDA 510(k) clearance for the TyFix™ all-in-one extremity fixation system. Jul 13, 2017
Pinnacle Spine Issued Patent for In Situ Graft Delivery Technology
Pinnacle Spine was granted U.S. Patent No. 9,649,203, Methods of Post-Filling an Intervertebral Implant. Jul 12, 2017
David Dvorak Departs as Zimmer Biomet CEO
Zimmer Biomet announced the departure of David Dvorak, its CEO of ten years. Dan Florin, Senior Vice President and CFO, will serve as interim CEO while the board seeks to fill the position. Jul 12, 2017
FDA 510(k) Clearance for Stryker RF Generator
Stryker received FDA 510(k) clearance for the MultiGen 2 RF Generator for radiofrequency ablation to treat facet joint pain. Jul 11, 2017
MedShape Launches DynaFrame CF Deployment System for TTC Fusion
MedShape launched DynaFrame™ CF, a carbon fiber-filled PEEK deployment system for use with DynaNail® TTC Fusion. Jul 11, 2017
CrossRoads Extremity Launches DynaFORCE Dynamic Compression Fixation
CrossRoads Extremity Systems launched DynaFORCE™ for foot/ankle procedures, reported to be the first hybrid fixation system on the market. Jul 11, 2017
Carmell Therapeutics Closes $4MM Series B Funding
Carmell Therapeutics closed a US $4MM Series B financing. Funds will support Phase III clinical development of the company’s Bone Healing Accelerant product. Jul 11, 2017
SeaSpine Reports Preliminary 2Q17 Revenue
SeaSpine announced preliminary 2Q17 revenue in the range of US $34.0MM to $34.2MM, +3% vs. 2Q16. Jul 11, 2017
