The following data is part of a premarket notification filed by Titan Spine, Llc with the FDA for Endoskeleton To.
| Device ID | K102067 |
| 510k Number | K102067 |
| Device Name: | ENDOSKELETON TO |
| Classification | Intervertebral Fusion Device With Bone Graft, Lumbar |
| Applicant | TITAN SPINE, LLC 13540 GUILD AVE Apple Valley, MN 55124 |
| Contact | Rich Jansen |
| Correspondent | Rich 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 | 2010-07-23 |
| Decision Date | 2010-11-05 |
| Summary: | summary |