The following data is part of a premarket notification filed by Astura Medical with the FDA for Alta Anterior Cervical Interbody Spacer.
Device ID | K160154 |
510k Number | K160154 |
Device Name: | ALTA Anterior Cervical Interbody Spacer |
Classification | Intervertebral Fusion Device With Bone Graft, Cervical |
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 | ODP |
CFR Regulation Number | 888.3080 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2016-01-20 |
Decision Date | 2016-05-13 |
Summary: | summary |