FDA 510(k) Applications Submitted by U&I CORP.

FDA 510(k) Number	Submission Date	Device Name	Applicant
K061002	04/11/2006	MAXIMA ANTERIOR CERVICAL PLATE SYSTEM	U&I CORP.
K051971	07/21/2005	OPTIMA SPINAL SYSTEM	U&I CORP.
K042928	10/22/2004	MODIFICATION TO GLOBAL SPINAL FIXATION SYSTEM	U&I CORP.
K132926	09/18/2013	VELOFIXTM INTERBODY FUSION SYSTEM	U&I CORP.
K120419	02/10/2012	DYNA LOCKING ANKLE NAIL	U&I CORP.
K112240	08/04/2011	DYNA LOCKING CANNULATED SCREW	U&I CORP.
K102367	08/20/2010	OPTIGEN TOTAL KNEE SYSTEM	U&I CORP.
K092771	09/09/2009	DYNA LOCKING IM NAIL	U&I CORP.
K093707	12/02/2009	DYNA LOCKING TROCHANTERIC NAIL, MODEL NG0820	U&I CORP.
K140864	04/03/2014	VELOXTM INTERBODY FUSION SYSTEM	U&I CORP.
K091725	06/11/2009	PERFIX SPINAL SYSTEM, MODEL SNA4530-9610, SNM4530-9610, SN3020 (TOTAL: 549)	U&I CORP.
K140234	01/29/2014	ASPIRON ACP SYSTEM	U&I CORP.