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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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