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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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