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 |