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Titan Spine, LLC

FDA 510(k) & PMA Approved Devices — 8 products

Total Devices8
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K173535 Endoskeleton® TAS Interbody Fusion Device, Endoskeleton® TAS Hyperlordotic Interbody Fusion Device and Endoskeleton® TCS Interbody Fusion DeviceODP2018-02-13 View
510(k) K170399 Endoskeleton TO Interbody Fusion Device (IBD)MAX2017-07-06 View
510(k) K163269 Endoskeleton(R) TAS Interbody Fusion Device / Endoskeleton(R) TAS Hyperlordotic Interbody Fusion DeviceOVD2017-04-13 View
510(k) K111626 ENDOSKELETON(R) TASOVD2011-09-09 View
510(k) K102067 ENDOSKELETON TOMAX2010-11-05 View
510(k) K100889 ENDOSKELETON TCODP2010-07-29 View
510(k) K083714 ENDOSKELETON TT INTERBODY FUSION DEVICE (IBD)MAX2009-04-15 View
510(k) K080615 ENDOSKELETON TA INTERBODY FUSION DEVICE (IBD)MAX2008-06-17 View
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