The FDA cleared 43 orthopedic- and spine-related devices in January.
Spinal Tech
NuVasive named two new members to their board of directors.
NuVasive's fourth quarter and full year revenue increased for 2015, and the company completed a key acquisition to boost 2016 financial performance.
Medline recently expanded its foot and ankle line to ensure its members have access to the latest products.
Zimmer Biomet received 510(k) clearance from the FDA for the Unite3D Bridge Fixation System.
RTI Surgical, Oxford Performance Materials enter into agreement for OsteoFab technology: 4 takeaways
RTI Surgical announced a new agreement with Oxford Performance Materials.
Here are 16 key notes on orthopedic and spine device companies over the past week.
SuitX, a California-based robotics company, won $1 million for its pediatric medical exoskeleton at the UAE Robotics for Good competition, according to eWeek.
San Jose, Calif.-based SI-BONE reported the National Government Services, the Medicare Administrative Contractor for Connecticut, Illinois, Maine, Massachusetts, Minnesota, New Hampshire, New York, Rhode Island, Vermont and Wisconsin, issued a positive local coverage determination for MIS SI joint fusion, effective…
On Feb. 11, the FDA released new draft guidance, helping Class II and III orthopedic device developers discern what type of information to include in their submissions for devices using ultrahigh molecular weight polyethylene material.
