Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Titan Spine, Inc.

FDA 510(k) & PMA Approved Devices — 5 products

Total Devices5
Categories3
Latest Approval2020-01-08
TypeNumberDevice NameCodeDate
510(k) K191581 Endoskeleton TL Interbody Fusion Device, Endoskeleton TL Hyperlordotic Interbody Fusion Device OVD 2020-01-08 View
510(k) K192054 Endoskeleton TAS Plate OVD 2019-08-29 View
510(k) K192018 Endoskeleton TA Interbody Fusion Device, Endoskeleton TAS and TAS Hyperlordotic Interbody Fusion Device, Endoskeleton TO Interbody Fusion Device, Endoskeleton TT Interbody Fusion Device, Endoskeleton TC Interbody Fusion Device, Endoskeleton TCS Interbody Fusion Device, Endoskeleton TL Interbody Fusion Device ODP 2019-08-16 View
510(k) K191565 Endoskeleton TCS Interbody Fusion Device OVE 2019-08-06 View
510(k) K183557 Endoskeleton® TA Interbody Fusion Device, Endoskeleton® TAS Interbody Fusion Device, Endoskeleton® TO Interbody Fusion Device, Endoskeleton® TT Interbody Fusion Device, Endoskeleton® TC Interbody Fusion Device, Endoskeleton® TCS Interbody Fusion Device, Endoskeleton® TL Interbody Fusion Device, Endoskeleton® TA Vertebral Body Replacement (VBR) Device ODP 2019-02-11 View
↑