FDA 510(k) Applications Submitted by CHERYL FREDERICK

FDA 510(k) Number	Submission Date	Device Name	Applicant
K120096	01/12/2012	MULTIFIX P KNOTLESS FIXATION DEVICE	ARTHROCARE CORPORATION
K120791	03/15/2012	AMBIENT TURBOFLASH 90 IFS	ARTHOCARE CORPORATION
K170990	04/03/2017	Active Needle Endoscopic Treatment (ANET) Electrosurgical Applicator	Spiration, Inc.
K121306	05/01/2012	SMARTSTITCH M-CONNECTOR ULTRA SMARTSTITCH SUTURE DEVICE HANDLE SMARTSTITCH SUTURE DEVICE HANDLE	ARTHOCARE CORPORATION
K171492	05/22/2017	B7 2C Occlusion Balloon	Spiration, Inc.
K122652	08/31/2012	ARTHROCARE TURBINATOR WAND	ARTHROCARE CORPORATION
K123240	10/16/2012	SPEEDLOCK HIP KNOTLESS FIXATION IMPLANT	ARTHROCARE CORPORATION
K123268	10/19/2012	SMARTSTITCH PERFECTPASSER SYSTEM	ARTHOCARE CORPORATION