We were unable to process your request. Please try again later. If you continue to have this issue please contact customerservice@slackinc.com. A novel synthetic bone graft showed noninferiority to ...
Medtronic’s Infuse bone graft earned the FDA’s premarket approval for one- and two-level transforaminal lumbar interbody spinal fusions. The expanded approval allows use with PEEK and titanium ...
Back and neck pain are leading causes of disability in the United States. According to the Center for Disease Control and Prevention (CDC), back pain in the United States is the leading cause of days ...
We were unable to process your request. Please try again later. If you continue to have this issue please contact customerservice@slackinc.com. The FDA granted 510(k) clearance for Spinal Elements’ ...
Approval underscores Cerapedics' commitment to investing in evidence that brings scientific rigor to bone grafting for spinal fusion. WESTMINSTER, Colo., Sept. 24, 2024 /PRNewswire/ -- Cerapedics Inc.
WESTMINSTER, Colo., Dec. 17, 2025 /PRNewswire/ -- Cerapedics Inc., a global, commercial-stage orthopedics company dedicated to redefining the path to bone repair, today announced the publication of ...
Ventris Medical’s Backpack contains bone particles designed to promote bone regeneration and healing following spinal fusion surgery Ventris Medical received 510(k) clearance for its bone graft ...
So far this year, medtech companies and academic institutions are making key strides in spine biologics. From new product launches to research breakthroughs, here are the biggest developments to know: ...
Medtronic (NYSE: MDT) announced today that it received FDA premarket approval (PMA) for the use of its Infuse bone graft in TLIF procedures.
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