CTL Medical Receives FDA 510(k) Clearance for MATISSE ACIF Cage
CTL Medical received FDA 510(k) clearance to market the MATISSE™ titanium ACIF cage. Jul 26, 2017
Australia Regulatory Approval for Providence Medical’s DTRAX Cervical Fusion Devices
Providence Medical Technology was granted regulatory approval in Australia for DTRAX® cervical fusion devices. Jul 25, 2017
Vertera Spine Receives FDA 510(k) for COALESCE PEEK LIF Device
Vertera Spine received FDA 510(k) clearance to market the COALESCE™ interbody fusion device for ALIF, TLIF, PLIF and LLIF procedures. Jul 25, 2017
Spinal Kinetics Passes 50,000 Implants of M6 Artificial Disc
Spinal Kinetics passed the milestone of a combined 50,000 implantations of its M6© artificial cervical and lumbar discs. Jul 25, 2017
Anika Therapeutics Receives India Regulatory Approval for MONOVISC
Anika Therapeutics received regulatory approval in India for MONOVISC® viscosupplement to treat OA pain in all synovial joints. Jul 25, 2017
WishBone Medical Launches Exact Osteotomy System
WishBone Medical introduced the Exact Osteotomy System, designed to support precise, repeatable bone cuts for all types of pediatric orthopaedic procedures. Jul 25, 2017
Paragon 28 Launches JAWS Nitinol Staple
Paragon 28 launched JAWS™, a Nitinol staple for use in osteotomy, arthrodesis and fragment fixation in the foot. Jul 25, 2017
OsteoRemedies, Adhezion Biomedical Enter Distribution Agreement
Adhezion Biomedical entered into an exclusive U.S. distribution agreement with OsteoRemedies for FLORASEAL® Microbial Sealant. Jul 25, 2017
First DenerveX Cases in Germany
Medovex scheduled first cases in Germany for its DenerveX™ device to treat Facet Joint Syndrome. Jul 25, 2017
Trauma and Spine Markets Gain New FDA Clearances
In 1H17, 23 orthopaedic companies from 11 countries received their first 510(k), according to FDA. We call your attention to these companies to assist you with identifying startups, as well as ex-U.S. companies entering the U.S. market. Jul 21, 2017
