The following data is part of a premarket notification filed by Titan Spine, Llc with the FDA for Endoskeleton Ta Interbody Fusion Device (ibd).
| Device ID | K080615 |
| 510k Number | K080615 |
| Device Name: | ENDOSKELETON TA INTERBODY FUSION DEVICE (IBD) |
| Classification | Intervertebral Fusion Device With Bone Graft, Lumbar |
| Applicant | TITAN SPINE, LLC 10520 BAEHR RD Mequon, WI 53092 |
| Contact | Kevin Gemas |
| Correspondent | Kevin Gemas TITAN SPINE, LLC 10520 BAEHR RD Mequon, WI 53092 |
| Product Code | MAX |
| CFR Regulation Number | 888.3080 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2008-03-04 |
| Decision Date | 2008-06-17 |
| Summary: | summary |