FDA 510(k) Applications Submitted by S. MICHAEL SHARP

FDA 510(k) Number Submission Date Device Name Applicant
K080936 04/02/2008 CONFORMIS TOTAL KNEE REPIAR SYSTEM (ITOTAL) TIBIAL COMPONENT: 6.0 MM THICKNESS CONFORMIS, INC.
K101017 04/12/2010 ANGIODYNAMICS, INC., SMART PORT CT SERIES PORT ACCESS SYSTEMS ANGIODYNAMICS, INC.
K061392 05/19/2006 IKONISCOPE FASTFISH AUTO/AMNIOCYTE TEST SYSTEM IKONISYS INC
K072586 09/13/2007 CONFORMIS UNI-CONDYLAR KNEE SYSTEM CONFORMIS, INC.
K052577 09/19/2005 IKONISCOPE FASTFISH AMNIO IMAGING SYSTEM IKONISYS INC


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