FDA 510(k) Applications Submitted by Jane Rodd
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K170399 |
02/09/2017 |
Endoskeleton TO Interbody Fusion Device (IBD) |
Titan Spine, LLC |
| K151596 |
06/12/2015 |
Endoskeleton TCS Interbody Fusion Device |
TITAN SPINE, LLC |
| K192018 |
07/29/2019 |
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 |
Titan Spine, Inc |
| K142589 |
09/15/2014 |
Endoskeleton TA IBD and VBR, Endoskeleton TO and TT, Endoskeleton TAS, Endoskeleton TAS, Endoskeleton TC, Endoskeleton TL |
TITAN SPINE, LLC |
| K142940 |
10/09/2014 |
Endoskeleton TCS System |
TITAN SPINE, LLC |
| K153122 |
10/29/2015 |
Endoskeleton(r) TCS System |
TITAN SPINE, LLC |
| K173535 |
11/15/2017 |
Endoskeleton« TAS Interbody Fusion Device, Endoskeleton« TAS Hyperlordotic Interbody Fusion Device and Endoskeleton« TCS Interbody Fusion Device |
Titan Spine, LLC |
| K163269 |
11/21/2016 |
Endoskeleton(R) TAS Interbody Fusion Device / Endoskeleton(R) TAS Hyperlordotic Interbody Fusion Device |
TITAN SPINE, LLC |
| K183557 |
12/20/2018 |
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, E |
Titan Spine, Inc |
|
|
