FDA 510(k) Applications Submitted by Titan Spine, Inc
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| 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 |
| 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 |
| K191565 |
06/13/2019 |
Endoskeleton TCS Interbody Fusion Device |
Titan Spine, Inc |
| K191581 |
06/14/2019 |
Endoskeleton TL Interbody Fusion Device, Endoskeleton TL Hyperlordotic Interbody Fusion Device |
Titan Spine, Inc |
| K192054 |
07/31/2019 |
Endoskeleton TAS Plate |
Titan Spine, Inc |
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