George Frey, MD, an orthopedic surgeon and founder of Mighty Oak Medical, recently shared a guiding system he developed to help surgeons precisely place screws in the vertebrae, according to a Denver Post report.
Spinal Tech
EDGE Orthopaedics received 510(k) clearance from the U.S. Food and Drug Administration for the VIEW Plating System and REDUCE Fracture Plating System.
Morristown, N.J.-based Tyber Medical rolled out its headless cannulated trauma screw system, which will be available to private label partners and surgeon advisors.
NuVasive Spine Foundation has contributed $13 million since its inception in 2009 and donated around $10.5 million worth of products.
Mazor Robotics announced that the China Food and Drug Administration approved its Renaissance surgical guidance system.
Orchid Orthopedic Solutions received a $300,000 state grant from the Michigan Economic Development Corporation, according to a Lansing State Journal report.
Titan Spine now offers a warranty for its Endoskeleton line of spinal interbody fusion devices for a one-time free replacement.
The United States filed two complaints under the False Claims Act related to physician-owned distributorships.
The Food and Drug Administration granted 39 orthopedic- and spine-related device clearances in August.
Ceterix Orthopaedics announced the issuance of a new patent adding to the company's existing patent portfolio.
