FDA 510(k) Applications Submitted by LIZ DOLAN

FDA 510(k) Number Submission Date Device Name Applicant
K033395 10/23/2003 CODMAN DURAL GRAFT IMPLANT, MODELS 80-1471, 80-1472, 80-1473, 80-1474, 80-1475, 80-1476, 80-1477, 80-1478, 80-1480, 80-1 Codman & Shurtleff, Inc.


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