BELGRADE, Mont., March 03, 2016 (GLOBE NEWSWIRE) -- Xtant Medical Holdings, Inc. (NYSE MKT:XTNT), a leader in the development of regenerative medicine products and medical devices, today announced CE clearance for its products Aranax™ and Irix-A™.
The Aranax™ Cervical Plating System is distributed as a pre-sterilized, ready-to-use implant. The Irix-A™ stand alone anterior lumbar fusion device consists of an integrated titanium ring, surrounded by a PEEK shell. The CE mark is mandatory for the distribution of medical devices in Europe.
"We are very pleased to have received these additional clearances for our best in class medical devices," said Dr. David Kirschman, Executive Vice President and Chief Scientific Officer of Xtant Medical. "They will allow us to expand our distribution presence and better serve the surgical needs of our customers internationally."
Xtant Medical is currently presenting these products, as well as its entire orthopedic portfolio, at the AAOS Annual Meeting in Orlando, Florida, booth 4113.
About Xtant Medical Holdings
Xtant Medical Holdings, Inc. (NYSE MKT:XTNT) develops, manufactures and markets class-leading regenerative medicine products and medical devices for domestic and international markets. Xtant products serve the specialized needs of orthopedic and neurological surgeons, including orthobiologics for the promotion of bone healing, implants and instrumentation for the treatment of spinal disease, tissue grafts for the treatment of orthopedic disorders, and biologics to promote healing following cranial, and foot and ankle surgeries. With core competencies in both biologic and non-biologic surgical technologies, Xtant can leverage its resources to successfully compete in global neurological and orthopedic surgery markets. For further information, please visit www.xtantmedical.com.
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Published at Nasdaq GlobeNewswire