Titan Spine, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Endoskeleton TL Interbody Fusion Device, Endoskeleton TL Hyperlordotic Interbody Fusion Device, Endoskeleton TAS Plate, 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
5
Total
5
Cleared
0
Denied
FDA 510(k) Regulatory Record - Titan Spine, Inc. Orthopedic ✕
5 devices
Cleared
Jan 08, 2020
Endoskeleton TL Interbody Fusion Device, Endoskeleton TL Hyperlordotic...
Orthopedic
208d
Cleared
Aug 29, 2019
Endoskeleton TAS Plate
Orthopedic
29d
Cleared
Aug 16, 2019
Endoskeleton TA Interbody Fusion Device, Endoskeleton TAS and TAS...
Orthopedic
18d
Cleared
Aug 06, 2019
Endoskeleton TCS Interbody Fusion Device
Orthopedic
54d
Cleared
Feb 11, 2019
Endoskeleton® TA Interbody Fusion Device, Endoskeleton® TAS Interbody Fusion...
Orthopedic
53d