The following data is part of a premarket notification filed by Premia Spine Ltd. with the FDA for Promis Fixation System.
| Device ID | K150380 |
| 510k Number | K150380 |
| Device Name: | ProMIS Fixation System |
| Classification | Thoracolumbosacral Pedicle Screw System |
| Applicant | Premia Spine Ltd. 7 Giborey Israel Street Ramat Poleg, IL 42504 |
| Contact | Ron Sacher |
| Correspondent | Ron Sacher Premia Spine Ltd. 7 Giborey Israel Street Ramat Poleg, IL 42504 |
| Product Code | NKB |
| 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 | 2015-02-13 |
| Decision Date | 2015-07-17 |
| Summary: | summary |