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 | K163481 |
510k Number | K163481 |
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 | Troy Taylor |
Correspondent | Troy Taylor Astura Medical 5670 El Camino Real Suite B Carlsbad, CA 92008 |
Product Code | MAX |
CFR Regulation Number | 888.3080 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2016-12-12 |
Decision Date | 2017-05-03 |
Summary: | summary |