K2M Gains FDA Clearance, CE Mark Approval for CAYMAN United Plate
K2M received FDA 510(k) clearance and CE Mark approval for the CAYMAN® United Plate. Jul 17, 2018
Vallum Gains FDA Clearance of Nanotextured PEEK Interbody
Vallum received FDA 510(k) clearance to market a PEEK interbody fusion device with a PEEKplus® nanotextured surface created with proprietary Accelerated Neutral Atom Beam technology. Jul 17, 2018
NuVasive Launches Reline Low-Profile Modular Implants
NuVasive introduced the Reline® MAS® Midline® cortical pedicle screw system for posterior fixation. Jul 16, 2018
Cartiva Synthetic Cartilage Implant Long-Term Clinical Data
Five-year follow-up results demonstrate that Cartiva's Synthetic Cartilage Implant provided long-term durability in pain and functional improvements in the treatment of great toe arthritis. Jul 16, 2018
Artoss Completes $1MM Funding Round
Artoss completed a US $1MM funding round. Proceeds will support development of new NanoBone® bone graft products for the U.S. market, regulatory requirements and commercialization. Jul 16, 2018
Cerapedics Closes $22MM Financing
Cerapedics completed a US $22MM financing. Proceeds will support commercialization and a U.S. lumbar trial of i-FACTOR bone graft. Jul 16, 2018
Aziyo Partners with SurGenTec for Minimally Invasive Bone Graft Delivery
Aziyo Biologics entered into an agreement to supply ViBone viable bone matrix for distribution with SurGenTec's GraftGun delivery system. Jul 13, 2018
Life Spine Launches CENTRIC-T Pedicle-Based Retractor
Life Spine commenced limited launch and announced first clinical use of the CENTRIC®-T Pedicle-Based Retractor for minimally invasive TLIF. Jul 13, 2018
OrthoPediatrics Launches Pediatric Nailing Platform | FEMUR
OrthoPediatrics commenced full U.S. launch of the Pediatric Nailing Platform | FEMUR rigid IM nail. Jul 11, 2018
Cutting Edge Spine Gains FDA Clearance for EVOL ha-C Interbody
Cutting Edge Spine received FDA 510(k) clearance to market the EVOL ha-C cervical interbody system. Jul 11, 2018
