Titan Spine, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
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
Titan Spine, Inc. has 5 FDA 510(k) cleared medical devices. Based in Mequon, US.
Historical record: 5 cleared submissions from 2019 to 2020. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Titan Spine, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Mrc/X, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Titan Spine, Inc.
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