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FDA 510(k) Applications Submitted by TRANS1 INCORPORATED
FDA 510(k) Number
Submission Date
Device Name
Applicant
K100210
01/25/2010
TRANS1 LATERAL INTERVERTEBRAL FUSION DEVICE, T
TRANS1 INCORPORATED
K092124
07/15/2009
AXIALIF 2L, AXIALIF 2-LEVEL SYSTEM, AXIALIF APOLLO, AXIALIF II
TRANS1 INCORPORATED
K102334
08/17/2010
TRANS1 AXIALIF PLUS
TRANS1 INCORPORATED
K120991
04/02/2012
TRANS1 INTERBODY FUSION SYSTEM
TRANS1 INCORPORATED
K073643
12/26/2007
TRANS1 AXIALIF 2-LEVEL OR II SYSTEM
TRANS1 INCORPORATED
K050965
04/18/2005
TRANS1 AXIALIF SYSTEM
TRANS1 INCORPORATED
K051856
07/08/2005
TRANS1 FACET SCREWS
TRANS1 INCORPORATED
K073514
12/14/2007
TRANS1 AXIAL FIXATON SYSTEM
TRANS1 INCORPORATED
K073515
12/14/2007
TRANS1 FACET SCREW
TRANS1 INCORPORATED
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