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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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