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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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