The following data is part of a premarket notification filed by Titan Spine, Llc with the FDA for Endoskeleton Tt Interbody Fusion Device (ibd).
| Device ID | K083714 |
| 510k Number | K083714 |
| Device Name: | ENDOSKELETON TT INTERBODY FUSION DEVICE (IBD) |
| Classification | Intervertebral Fusion Device With Bone Graft, Lumbar |
| Applicant | TITAN SPINE, LLC 13540 GUILD AVE Apple Valley, MN 55124 |
| Contact | Richard Jansen |
| Correspondent | Richard Jansen TITAN SPINE, LLC 13540 GUILD AVE Apple Valley, MN 55124 |
| Product Code | MAX |
| CFR Regulation Number | 888.3080 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2008-12-15 |
| Decision Date | 2009-04-15 |
| Summary: | summary |