The following data is part of a premarket notification filed by Alphatec Spine, Inc. with the FDA for Novel Spinal Spacer System.
Device ID | K080699 |
510k Number | K080699 |
Device Name: | NOVEL SPINAL SPACER SYSTEM |
Classification | Spinal Vertebral Body Replacement Device |
Applicant | ALPHATEC SPINE, INC. 2051 PALOMAR AIRPORT ROAD SUITE 100 Carlsbad, CA 92011 |
Contact | Mary Stanners |
Correspondent | Mary Stanners ALPHATEC SPINE, INC. 2051 PALOMAR AIRPORT ROAD SUITE 100 Carlsbad, CA 92011 |
Product Code | MQP |
CFR Regulation Number | 888.3060 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2008-03-12 |
Decision Date | 2008-05-21 |
Summary: | summary |