FDA 510(k) Applications Submitted by ArthoCare Corporation

FDA 510(k) Number Submission Date Device Name Applicant
K120791 03/15/2012 AMBIENT TURBOFLASH 90 IFS ARTHOCARE CORPORATION
K121306 05/01/2012 SMARTSTITCH M-CONNECTOR ULTRA SMARTSTITCH SUTURE DEVICE HANDLE SMARTSTITCH SUTURE DEVICE HANDLE ARTHOCARE CORPORATION
K123268 10/19/2012 SMARTSTITCH PERFECTPASSER SYSTEM ARTHOCARE CORPORATION
K153669 12/21/2015 MultiFIX S Ultra Knotless Fixation System ArthoCare Corporation
K131182 04/26/2013 MULTIFIX S KNOTLESS FIXATION DEVICE ARTHOCARE CORPORATION
K013334 10/09/2001 ENDOFLIP ARTHOCARE CORPORATION


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