The following data is part of a premarket notification filed by Titan Spine, Llc with the FDA for Endoskeleton Tcs System.
| Device ID | K142940 |
| 510k Number | K142940 |
| Device Name: | Endoskeleton TCS System |
| Classification | Intervertebral Fusion Device With Integrated Fixation, Cervical |
| Applicant | TITAN SPINE, LLC 6140 WEST EXECUTIVE DRIVE, SUITE A Mequon, WI 53092 |
| Contact | Jane Rodd |
| Correspondent | Christine Scifert MEMPHIS REGULATORY CONSULTING, LLC 3416 ROXEE RUN COVE Bartlette, TN 38133 |
| Product Code | OVE |
| CFR Regulation Number | 888.3080 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2014-10-09 |
| Decision Date | 2015-01-28 |
| Summary: | summary |