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 |