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February 6, 2014
07:40 EDTCOVCovidien receives FDA 510(k) clearance for Reinforced Stapling Reload technology
Covidien announced that the U.S. Food and Drug Administration has granted 510(k) clearance for the companyís Endo GIAReinforced Reload with Tri-Staple technology. This clearance extends Covidienís industry-leading portfolio of advanced surgical staplers and represents a return by the company to the U.S. market for surgical staplers that integrate buttress material for additional tissue support.
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