FDA 510(k) Applications Submitted by LESTER PADILLA

FDA 510(k) Number	Submission Date	Device Name	Applicant
K093312	10/22/2009	KIMBERLY-CLARK GASTROINTESTINAL ANCHOR SET WITH SAF-T-PEXY FASTENERS, ENTERNAL ACCESS DILATION SYSTEM	KIMBERLY-CLARK CORP.
K060121	01/17/2006	BIOMET PRE-CALIBRATED COMPUTER AIDED SURGERY NAVIGATION INSTRUMENTS FOR HIP APPLICATIONS	BIOMET MANUFACTURING CORP.
K060693	03/15/2006	MICROSTRIKE AND ALLTHREAD PEEK SUTURE ANCHOR	ARTHROTEK, INC.
K061340	05/15/2006	23 MM SINGLE-PEG PATELLA COMPONENT	BIOMET MANUFACTURING, INC.
K061389	05/18/2006	ALLTHREAD LACTOSORB SUTURE ANCHOR	ARTHROTEK, INC.
K101596	06/08/2010	KIMBERLY-CLARK PURPLE NITRILE POWDER-FREE EXAM GLOVE (CHEMOTHERAPY GLOVE) AND KIMBERLY-CLARK PURPLE NITRILE XTRA POWDER-	KIMBERLY-CLARK
K061657	06/13/2006	HITCH LACTOSORB SUTURE ANCHOR	ARTHROTEK, INC.
K061681	06/15/2006	REPICCI II METAL BACK INLAY UNICOMPARTMENTAL TIBIAL BEARING COMPONENT	BIOMET MANUFACTURING CORP.
K102032	07/19/2010	KIMBERLY-CLARK PURPLE NITRILE XTRA* STERILE POWDER-FREE EXAM GLOVE (CHEMOTHERAPY GLOVE) - 12 STERILE PAIRS	KIMBERLY-CLARK CORP.
K052990	10/24/2005	STAGEONE DISPOSABLE CEMENT SPACER MOLD FOR TEMPORARY HIP PROSTHESIS WITH REINFORCEMENT STEM	BIOMET, INC.
K113423	11/21/2011	KIMBERLY CLARK PURPLE NITRILE, AND PURPLE NITRILE XTRA POWDER FREE EXAM GLOVE	KIMBERLY-CLARK CORP.