The following data is part of a premarket notification filed by Alphatec Spine, Inc. with the FDA for Zodic Polyaxial Spinal Fixation System.
Device ID | K081158 |
510k Number | K081158 |
Device Name: | ZODIC POLYAXIAL SPINAL FIXATION SYSTEM |
Classification | Orthosis, Spinal Pedicle Fixation |
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 | MNI |
Subsequent Product Code | KWP |
Subsequent Product Code | MNH |
CFR Regulation Number | 888.3070 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2008-04-23 |
Decision Date | 2008-07-03 |
Summary: | summary |