January 3, 2017 – By BRAD PERRIELLO Fresh from the sale last August of Domain Surgical to OmniGuide Surgical, former Domain CEO David McNally landed the top spot at Titan Medical (CVE:TMD), that company said today. McNally, who also founded and led Zevex International to a 2007 acquisition by Moog Inc., succeeded interim chief John Barker effective Jan. 1. […]
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TUCSON, Ariz., Jan. 3, 2017 /PRNewswire-USNewswire/ — The right to contract is fundamental, and the Association of American Physicians and Surgeons (AAPS) applauds the strong defense of that right by Florida Supreme Court Justice Charles Canady. He is on the list of candidates being considered by President-elect Donald Trump for nomination to the U.S. Supreme Court. […]
Elizabeth Hofheinz, M.P.H., M.Ed. • Tue, December 27th, 2016 For many years the standard in training airline pilots has been pre-flight simulators. This helps them become more skilled at flying the actual plane. This is a comfortable thought isn’t it? Exactly! Well, recent developments in shoulder replacement surgery allow surgeons to simulate surgery and this […]
BY MAURY THOMPSON, THE POST-STAR, GLENS FALLS, N.Y. / DECEMBER 28, 2016 (TNS) — The federal Food and Drug Administration has required medical companies testing new products to get permission from multiple separate regional FDA review boards across the country wherever test subjects live. Legislation that President Barack Obama signed earlier this month will allow […]
By Jof Enriquez – December 29, 2016 The U.S. Food and Drug Administration (FDA) Center for Devices and Radiological Health (CDRH) has posted the lists of medical device guidance documents it will prioritize for fiscal year 2017, pursuant to the Medical Device User Fee Amendments of 2012 (MDUFA III) (Public Law 112-114). CDRH provides three lists: (1) […]
SAN DIEGO, CA–(Marketwired – December 29, 2016) – NuVasive, Inc. (NUVA), a leading medical device company focused on transforming spine surgery with minimally disruptive, procedurally-integrated solutions, today announced it received approval for instruments used in the eXtreme Lateral Interbody Fusion (XLIF®) procedure by the Japanese Ministry of Health, Labour and Welfare (MHLW). Recent guidance from […]
Maury Thompson, The Post-Star, Glen Galls, N.Y – December 29, 2016 (TNS) — The federal Food and Drug Administration has required medical companies testing new products to get permission from multiple separate regional FDA review boards across the country wherever test subjects live. Legislation that President Barack Obama signed earlier this month will allow medical […]
Elizabeth Hofheinz, M.P.H., M.Ed. • Tue, December 27th, 2016 For many years the standard in training airline pilots has been pre-flight simulators. This helps them become more skilled at flying the actual plane. This is a comfortable thought isn’t it? Exactly! Well, recent developments in shoulder replacement surgery allow surgeons to simulate surgery and this […]
By Jof Enriquez – December 29, 2016 The U.S. Food and Drug Administration (FDA) Center for Devices and Radiological Health (CDRH) has posted the lists of medical device guidance documents it will prioritize for fiscal year 2017, pursuant to the Medical Device User Fee Amendments of 2012 (MDUFA III) (Public Law 112-114). CDRH provides three lists: (1) […]
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