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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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