FDA 510(k) Applications Submitted by Samantha Passman

FDA 510(k) Number Submission Date Device Name Applicant
K201132 04/28/2020 Arthrex Compression Screws Arthrex Inc.
K203239 11/03/2020 Arthrex Low Profile Screws Arthrex Inc.
K203294 11/09/2020 Arthrex Pilon Fusion System Arthrex Inc.


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact