FDA 510(k) Applications Submitted by LESTER F 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.


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