The following data is part of a premarket notification filed by Alphatec Spine, Inc with the FDA for Solanas® Posterior Stabilization System.
| Device ID | K173522 |
| 510k Number | K173522 |
| Device Name: | Solanas® Posterior Stabilization System |
| Classification | Thoracolumbosacral Pedicle Screw System |
| Applicant | Alphatec Spine, Inc 5818 El Camino Real Carlsbad, CA 92008 |
| Contact | Natalia Shirina |
| Correspondent | Natalia Shirina Alphatec Spine, Inc 5818 El Camino Real Carlsbad, CA 92008 |
| Product Code | NKB |
| CFR Regulation Number | 888.3070 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2017-11-14 |
| Decision Date | 2017-11-30 |
| Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() SOLANAS 77181251 3391172 Live/Registered |
Alphatec Spine, Inc. 2007-05-15 |