The following data is part of a premarket notification filed by Titan Spine, Llc with the FDA for Endoskeleton Tc.
| Device ID | K100889 |
| 510k Number | K100889 |
| Device Name: | ENDOSKELETON TC |
| Classification | Intervertebral Fusion Device With Bone Graft, Cervical |
| Applicant | TITAN SPINE, LLC 555 13TH ST, NW Washington, DC 20004 |
| Contact | John J Smith |
| Correspondent | John J Smith TITAN SPINE, LLC 555 13TH ST, NW Washington, DC 20004 |
| Product Code | ODP |
| CFR Regulation Number | 888.3080 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2010-03-31 |
| Decision Date | 2010-07-29 |
| Summary: | summary |