Titan Spine, LLC
FDA 510(k) & PMA Approved Devices — 3 products
Total Devices3
Categories3
Latest Approval2018-02-13
| Type | Number | Device Name | Code | Date | |
|---|---|---|---|---|---|
| 510(k) | K173535 | Endoskeleton® TAS Interbody Fusion Device, Endoskeleton® TAS Hyperlordotic Interbody Fusion Device and Endoskeleton® TCS Interbody Fusion Device | ODP | 2018-02-13 | View |
| 510(k) | K170399 | Endoskeleton TO Interbody Fusion Device (IBD) | MAX | 2017-07-06 | View |
| 510(k) | K163269 | Endoskeleton(R) TAS Interbody Fusion Device / Endoskeleton(R) TAS Hyperlordotic Interbody Fusion Device | OVD | 2017-04-13 | View |
No matching devices.