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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.
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