FDA 510(k) Applications Submitted by Paragon 28

FDA 510(k) Number Submission Date Device Name Applicant
K172886 09/21/2017 Breakaway Screw System Paragon 28
K170923 03/29/2017 JAWS(TM) Nitinol Staple System Paragon 28
K151418 05/28/2015 Monster Screw System PARAGON 28
K171715 06/09/2017 HammerTube System Paragon 28
K162241 08/10/2016 TITAN 3-DÖ Wedge System PARAGON 28
K153378 11/23/2015 Monster BITE Screw System PARAGON 28
K140397 02/18/2014 PARALOCK PLATING SYSTEM / TUFFNEK SCREW PARAGON 28


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