Titan Spine, LLC is one of 13745 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Titan Spine, LLC - FDA 510(k) Cleared Devices
Recent clearances: Endoskeleton® TAS Interbody Fusion Device, Endoskeleton® TAS Hyperlordotic Interbody Fusion Device and Endoskeleton® TCS Interbody Fusion Device, Endoskeleton TO Interbody Fusion Device (IBD), Endoskeleton(R) TAS Interbody Fusion Device / Endoskeleton(R) TAS Hyperlordotic Interbody Fusion Device
14
Total
14
Cleared
0
Denied
Titan Spine, LLC has 14 FDA 510(k) cleared orthopedic devices. Based in Mequon, US.
Historical record: 14 cleared submissions from 2008 to 2018.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Memphis Regulatory Consulting, LLC, Mrc/X, LLC and Mrc-X, LLC.
FDA 510(k) Regulatory Record - Titan Spine, LLC
14 devices
Cleared
Feb 13, 2018
Endoskeleton® TAS Interbody Fusion Device, Endoskeleton® TAS Hyperlordotic...
Orthopedic
90d
Cleared
Jul 06, 2017
Endoskeleton TO Interbody Fusion Device (IBD)
Orthopedic
147d
Cleared
Apr 13, 2017
Endoskeleton(R) TAS Interbody Fusion Device / Endoskeleton(R) TAS...
Orthopedic
143d
Cleared
Dec 14, 2015
Endoskeleton(r) TCS System
Orthopedic
46d
Cleared
Oct 09, 2015
Endoskeleton TCS Interbody Fusion Device
Orthopedic
119d
Cleared
Jan 28, 2015
Endoskeleton TCS System
Orthopedic
111d
Cleared
Oct 27, 2014
ENDOSKELETON
Orthopedic
101d
Cleared
Oct 17, 2014
Endoskeleton TA IBD and VBR, Endoskeleton TO and TT, Endoskeleton TAS,...
Orthopedic
32d
Cleared
Jul 02, 2014
ENDOSKELETON(R) TL INTERBODY FUSION DEVICE
Orthopedic
173d
Cleared
Sep 09, 2011
ENDOSKELETON(R) TAS
Orthopedic
91d
Cleared
Nov 05, 2010
ENDOSKELETON TO
Orthopedic
105d
Cleared
Jul 29, 2010
ENDOSKELETON TC
Orthopedic
120d