免责声明: 本站汇总 FDA、ClinicalTrials.gov、PubMed、SEC EDGAR 等官方公开数据，仅供一般参考，不构成医疗建议、诊断、治疗建议或投资建议。

Titan Spine, Inc.

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

器械总数5
类别0
最新FDA决定
类型编号器械名称代码日期操作
510(k) K191581 Endoskeleton TL Interbody Fusion Device, Endoskeleton TL Hyperlordotic Interbody Fusion DeviceOVD2020-01-08 查看
510(k) K192054 Endoskeleton TAS PlateOVD2019-08-29 查看
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 DeviceODP2019-08-16 查看
510(k) K191565 Endoskeleton TCS Interbody Fusion DeviceOVE2019-08-06 查看
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) DeviceODP2019-02-11 查看
↑