FDA 510(k) Applications Submitted by BERNARD F GRISONI

FDA 510(k) Number Submission Date Device Name Applicant
K000019 01/04/2000 SINGLE SIZE TENDON SPACER MEDIST INTERNATIONAL
K031838 06/16/2003 PROFUSION BONE VOID FILLER KIT BIOGENERATION
K973704 09/29/1997 PROFUSION BONE VOID FILLER BIOGENERATION


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