The FDA granted 510(k) clearance to Ascendx Spine for its VCF Repair System for vertebral compression fractures.
Spinal Tech
San Jose, Calif.-based medical device company SI-BONE has a peer-reviewed journal article published on its iFuse Implant System.
Blue Belt Technologies' NavioPFS unicondylar knee replacement system has received FDA 510(k) clearance.
NuVasive has received Japanese clearance for its CoRoent Large Impacted and CoRoent Large Tapered titanium alloy spine implants.
Here are 12 orthopedic and spine device executive moves over the past few months.
Orthofix's investigation into its bone growth stimulation business has concluded, and the company will pay $43 million to fully resolve matters, both criminal and civil.
Medtronic has been training physicians on its devices in mobile labs for a decade, and now the company will release a new lab 2013, according to Commercial Appeal.
Gavin Fabian, CEO of MedPassage, discusses the medical device industry and trends for lowering costs in the future.
The Food and Drug Administration granted 16 spine-related clearances in November.
Morton Hospital in Taunton, Mass., has acquired a Robotic Arm Interactive Orthopedic System for partial knee replacement and total hip replacement procedures, according to the Taunton Daily Gazette.
