The following data is part of a premarket notification filed by Titan Spine, Llc with the FDA for Endoskeleton(r) Tas.
| Device ID | K111626 |
| 510k Number | K111626 |
| Device Name: | ENDOSKELETON(R) TAS |
| Classification | Intervertebral Fusion Device With Integrated Fixation, 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 | OVD |
| CFR Regulation Number | 888.3080 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2011-06-10 |
| Decision Date | 2011-09-09 |
| Summary: | summary |