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ArthroCare, a maker of minimally invasive surgical products, has received FDA clearance for its second-generation Parallax Contour-enhanced vertebral augmentation device, according to a news release.
VySpine’s VyBrate VBR system earned the FDA’s 510(k) clearance, according to a Jan. 13 news release. The device combines the osseointegration properties of the OXPEKK material and the OsteoVy lattice ...
Please provide your email address to receive an email when new articles are posted on . Published results showed a significant proportion of patients with vertebral compression fractures had decreased ...
Dr. Ari Salis, the director of interventional radiology and chairman of radiology at Concord Hospital, discusses interventional radiology and how it can help treat vertebral compression fractures. An ...
FDA clearance confirms robust safety and performance of VCFix® Spinal System, a breakthrough treatment for vertebral compression fractures US commercial pilot launch planned for early 2026, followed ...
DUBLIN, Sept. 16, 2019 (GLOBE NEWSWIRE) -- Medtronic plc (NYSE:MDT), the global leader in medical technology, today announced that the National Osteoporosis Foundation (NOF) supports the VCF Care ...
NEW YORK--(BUSINESS WIRE)--AgNovos Healthcare, a developer of medical technology products leveraging regenerative medicine to treat the local effects of bone disease, announced today that its newest ...