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 |