The following data is part of a premarket notification filed by Alphatec Spine with the FDA for Solanas® Posterior Oct Fixation System.
Device ID | K191185 |
510k Number | K191185 |
Device Name: | Solanas® Posterior OCT Fixation System |
Classification | Posterior Cervical Screw System |
Applicant | Alphatec Spine 5818 El Camino Real Carlsbad, CA 92008 |
Contact | Ruby Zheng |
Correspondent | Ruby Zheng Alphatec Spine 5818 El Camino Real Carlsbad, CA 92008 |
Product Code | NKG |
CFR Regulation Number | 888.3075 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2019-05-03 |
Decision Date | 2019-06-03 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
SOLANAS 77181251 3391172 Live/Registered |
Alphatec Spine, Inc. 2007-05-15 |