FDA 510(k) Applications Submitted by DONNA COLEMAN

FDA 510(k) Number	Submission Date	Device Name	Applicant
K120787	03/15/2012	MERETE LOCKING BONE PLATE SYSTEM III	MERETE MEDICAL GMBH
K101939	07/12/2010	OSTEOBRIDGE IKA INTRAMEDULLARY KNEE ARTHRODESIS ROD FIXATION SYSTEM	MERETE MEDICAL GMBH
K072251	08/13/2007	MERETE TOEMOBILE ANATOMICAL GREAT TOE RESURFACING SYSTEM	MERETE MEDICAL GMBH
K063487	11/17/2006	MERETE BLP SMALL FRAGMENT LOCKING BONE PLATE	MERETE MEDICAL GMBH