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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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