FDA 510(k) Applications Submitted by Stewart B. Davis

FDA 510(k) Number Submission Date Device Name Applicant
K093253 10/16/2009 AMID STAPLER SAFESTITCH LLC
K060151 01/20/2006 ORBITAL TISSUE EXPANDER (OTE) INNOVIA, LLC
K223244 10/20/2022 Pristine Arthroscopic Visualization System Pristine Surgical
K183165 11/15/2018 Pristine Scope Pristine Surgical
K193161 11/15/2019 Pristine Scope Pristine Surgical


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