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 |