The following data is part of a premarket notification filed by Amedica Corporation with the FDA for Preference Elite Pedicle Screw System.
| Device ID | K162160 |
| 510k Number | K162160 |
| Device Name: | Preference Elite Pedicle Screw System |
| Classification | Thoracolumbosacral Pedicle Screw System |
| Applicant | AMEDICA CORPORATION 1885 W 2100 S Salt Lake City, UT 84119 |
| Contact | Shanna Ryan |
| Correspondent | Shanna Ryan AMEDICA CORPORATION 1885 West 2100 South Salt Lake City, UT 84119 |
| Product Code | NKB |
| Subsequent Product Code | KWP |
| Subsequent Product Code | MNH |
| Subsequent Product Code | MNI |
| CFR Regulation Number | 888.3070 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2016-08-02 |
| Decision Date | 2016-11-18 |
| Summary: | summary |