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FDA 510(k) Applications Submitted by PETRA C SMIT
FDA 510(k) Number
Submission Date
Device Name
Applicant
K021953
06/13/2002
MITEK PDS/PGA STAPLE
MITEK WORLDWIDE
K023388
10/09/2002
MITEK RAPIDLOC-PDS MENISCAL REPAIR SYSTEM
MITEK WORLDWIDE
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