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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