MARQUETTE, Mich.--(BUSINESS WIRE)--Able Medical Devices announces that the MACH™ Screw Clip System has been granted 510k clearance by the FDA. The MACH Screw Clip System is a single-use, sterile screw ...

Plainsboro, N.J.-based Integra LifeSciences, a leader in regenerative medicine, has announced that the first surgery using Integra Spine’s Paramount Pedicle Screw System for minimally invasive spine ...

A recent press release by Mahe Medical USA announces it’s new spine emergency screw removal system at Becker’s 16th Annual Spine & Orthopedic Conference. “New universal system can remove any spine ...

SAN JOSE, Calif.--(BUSINESS WIRE)--Silver Bullet Therapeutics, Inc., a privately-held medical device company, announced today that it has received recommendation for CE Mark approval for the ...

OrthoPediatrics Corp. KIDS announced the limited launch or beta release of its Large Fragment Cannulated Screw System in the United States. Notably, this is the 34th surgical system from the company’s ...

Please provide your email address to receive an email when new articles are posted on . Neo Medical has announced an additional FDA 510(k) clearance of its pedicle screw system for advanced-stage ...

Please provide your email address to receive an email when new articles are posted on . Carbon22, a company of GLW Inc., has received FDA 510(k) clearance to market the Creed cannulated screw system, ...

MEMPHIS, Tenn.--(BUSINESS WIRE)-- Medtronic, Inc. (NYSE: MDT) today announced the European launch of the CD HORIZON ® Fenestrated Screw Spinal System, which is used in conjunction with Fenestrated ...

Small Bone Innovations, Inc. Receives US FDA 510(k) Clearance for Mini-Rail Fixation System and Large Cannulated Screw System NEW YORK--(BUSINESS WIRE)--Small Bone Innovations, Inc. (SBi), a leading, ...

AIS is the Most Common Type of Scoliosis Seen in Adolescents and Affects Nearly One Million Adolescents in the U.S. Alone MEMPHIS, Tenn.--(BUSINESS WIRE)-- Medtronic (NYSE: MDT) announced today it ...