FDA 510(k) Applications Submitted by Frank Pennesi

FDA 510(k) Number Submission Date Device Name Applicant
K200312 02/06/2020 Tryptik Ti Spineart
K140474 02/25/2014 JULIET OL SPINEART
K181203 05/07/2018 Juliet Ti Spineart
K122366 08/06/2012 TRYPTIK CC ANTERIOR INTERSOMATIC CERVICAL CAGE SPINEART


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