FDA 510(k) Applications Submitted by TITAN SPINE, LLC

FDA 510(k) Number Submission Date Device Name Applicant
K140055 01/10/2014 ENDOSKELETON(R) TL INTERBODY FUSION DEVICE TITAN SPINE, LLC
K141953 07/18/2014 ENDOSKELETON; TA IBD AND VBR, TO AND TT, TAS, TC, TL TITAN SPINE, LLC
K170399 02/09/2017 Endoskeleton TO Interbody Fusion Device (IBD) Titan Spine, LLC
K151596 06/12/2015 Endoskeleton TCS Interbody Fusion Device TITAN SPINE, LLC
K142589 09/15/2014 Endoskeleton TA IBD and VBR, Endoskeleton TO and TT, Endoskeleton TAS, Endoskeleton TAS, Endoskeleton TC, Endoskeleton TL TITAN SPINE, LLC
K142940 10/09/2014 Endoskeleton TCS System TITAN SPINE, LLC
K153122 10/29/2015 Endoskeleton(r) TCS System TITAN SPINE, LLC
K173535 11/15/2017 Endoskeleton« TAS Interbody Fusion Device, Endoskeleton« TAS Hyperlordotic Interbody Fusion Device and Endoskeleton« TCS Interbody Fusion Device Titan Spine, LLC
K163269 11/21/2016 Endoskeleton(R) TAS Interbody Fusion Device / Endoskeleton(R) TAS Hyperlordotic Interbody Fusion Device TITAN SPINE, LLC
K100889 03/31/2010 ENDOSKELETON TC TITAN SPINE, LLC
K080615 03/04/2008 ENDOSKELETON TA INTERBODY FUSION DEVICE (IBD) TITAN SPINE, LLC
K111626 06/10/2011 ENDOSKELETON(R) TAS TITAN SPINE, LLC
K102067 07/23/2010 ENDOSKELETON TO TITAN SPINE, LLC
K083714 12/15/2008 ENDOSKELETON TT INTERBODY FUSION DEVICE (IBD) TITAN SPINE, LLC


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