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FDA 510(k) Applications Submitted by DONNA M GARDNER
FDA 510(k) Number
Submission Date
Device Name
Applicant
K020110
01/11/2002
MODIFICATION TO TRELEX MESH SURGICAL MESH
BOSTON SCIENTIFIC
K030503
02/19/2003
MODIFICATION TO CONTOUR POLARIS URETERAL STENT
BOSTON SCIENTIFIC CORP.
K040787
03/29/2004
MODIFICATION TO SURGICAL MESH POLYMERIC
BOSTON SCIENTIFIC
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