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 |