Covidien Receives U.S. FDA 510(k) Clearance for Reinforced Stapling Reload Technology
DUBLIN, Ireland--(BUSINESS WIRE)--Feb. 6, 2014-- Covidien plc. (NYSE:COV) announced that the U.S. Food and Drug Administration has granted 510(k) clearance for the company’s Endo GIA™...
The Endo GIA Reinforced Reload -- the only endoscopic stapler featuring pre-loaded tissue reinforcement -- combines the benefits of Tri-Staple technology with a pre-attached synthetic, porous buttress material that provides additional support to fragile tissue that is being stapled and resected. All Covidien Endo GIA reloads with Tri-Staple technology are designed to work in harmony with the natural properties of tissue to optimize performance during stapling.
“Covidien is committed to developing specialized solutions for our customers that enable better patient outcomes,” said
The advanced polymer buttressing material is a version of NEOVEIL® felt, developed by
“Our Tri-Staple platform of stapling products represents the most successful product line in Covidien’s history,” said
In January,
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Sr. Director, Investor Relations
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