www.fdanews.com/articles/178295-orthosera-receives-ce-mark-for-hypact-device-to-restore-osteoarthritic-bone
OrthoSera Receives CE Mark for hypACT Device to Restore Osteoarthritic Bone
September 7, 2016
Austria-based orthobiologics company OrthoSera has received EU market authorization for its autologous hypACT injection device, which is available for clinical use.
The company has developed a hyperacute serum technology to be used to treat osteoarthritis and other degenerative diseases and is to be administered through the hypACT device.
The device isolates a specific serum derivative (SPRF) from the patient in a closed system, which is then applied during a same-day-procedure. — Cynthia Jessup