The following data is part of a premarket notification filed by Alphatec Spine, Inc. with the FDA for Novel Cervical Spinal Spacer System.
| Device ID | K081730 |
| 510k Number | K081730 |
| Device Name: | NOVEL CERVICAL SPINAL SPACER SYSTEM |
| Classification | Intervertebral Fusion Device With Bone Graft, Cervical |
| Applicant | ALPHATEC SPINE, INC. 2051 PALOMAR AIRPORT ROAD SUITE 100 Carlsbad, CA 92011 |
| Contact | Mary Scanners |
| Correspondent | Mary Scanners ALPHATEC SPINE, INC. 2051 PALOMAR AIRPORT ROAD SUITE 100 Carlsbad, CA 92011 |
| Product Code | ODP |
| CFR Regulation Number | 888.3080 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2008-06-18 |
| Decision Date | 2008-09-19 |
| Summary: | summary |