The following data is part of a premarket notification filed by Astura Medical with the FDA for Half Dome Posterior Lumbar Interbody System.
Device ID | K152512 |
510k Number | K152512 |
Device Name: | Half Dome Posterior Lumbar Interbody System |
Classification | Intervertebral Fusion Device With Bone Graft, Lumbar |
Applicant | Astura Medical 5670 El Camino Real, Suite B Carlsbad, CA 92008 |
Contact | Thomas Astura |
Correspondent | J D Webb The OrthoMedix Group, Inc. 1001 Oakwood Blvd Round Rock, TX 78681 |
Product Code | MAX |
CFR Regulation Number | 888.3080 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2015-09-02 |
Decision Date | 2016-01-28 |
Summary: | summary |