The following data is part of a premarket notification filed by Titan Spine, Inc with the FDA for Endoskeleton Tl Interbody Fusion Device, Endoskeleton Tl Hyperlordotic Interbody Fusion Device.
| Device ID | K191581 |
| 510k Number | K191581 |
| Device Name: | Endoskeleton TL Interbody Fusion Device, Endoskeleton TL Hyperlordotic Interbody Fusion Device |
| Classification | Intervertebral Fusion Device With Integrated Fixation, Lumbar |
| Applicant | Titan Spine, Inc 6140 W. Executive Dr., Suite A Mequon, WI 53092 |
| Contact | Kelly Mcdonnell |
| Correspondent | Christine Scifert Mrc/x, Llc 6075 Poplar Avenue Memphis, TN 38119 |
| Product Code | OVD |
| CFR Regulation Number | 888.3080 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2019-06-14 |
| Decision Date | 2020-01-08 |