FDA 510(k) Applications Submitted by KENSEY NASH CORPORATION

FDA 510(k) Number Submission Date Device Name Applicant
K061030 04/14/2006 BIOBLANKET SURGICAL MESH KENSEY NASH CORPORATION
K060917 04/04/2006 KENSEY NASH BONE VOID FILLER KENSEY NASH CORPORATION
K121310 05/01/2012 MESOTHELIUM DENTAL MEMBRANE KENSEY NASH CORPORATION
K112888 09/30/2011 MESO WOUND MATRIX KENSEY NASH CORPORATION
K094061 12/31/2009 KENSEY NASH ECM SURGICAL PATCH KENSEY NASH CORPORATION
K073162 11/09/2007 SAFE-CROSS(R) RADIO FREQUENCY TOTAL OCCLUSION CROSSING SYSTEM, SAFE-CROSS(R) RADIO FREQUENCY TOTAL OCCLUSION CROSSING KENSEY NASH CORPORATION


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