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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