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 |