The following data is part of a premarket notification filed by Astura Medical with the FDA for Zion Anterior Cervical Fixation System.
Device ID | K160702 |
510k Number | K160702 |
Device Name: | ZION Anterior Cervical Fixation System |
Classification | Appliance, Fixation, Spinal Intervertebral Body |
Applicant | Astura Medical 5670 El Camino Real, Suite B Carlsbad, CA 92008 |
Contact | Troy Taylor |
Correspondent | J.d Webb THE ORTHOMEDIX GROUP, INC 1001 OAKWOOD BLVD Round Rock, TX 78681 |
Product Code | KWQ |
CFR Regulation Number | 888.3060 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2016-03-14 |
Decision Date | 2016-08-23 |
Summary: | summary |