The following data is part of a premarket notification filed by Reliance Medical Systems, Llc with the FDA for Reliance Spinal Screw System.
Device ID | K152131 |
510k Number | K152131 |
Device Name: | Reliance Spinal Screw System |
Classification | Orthosis, Spinal Pedicle Fixation |
Applicant | Reliance Medical Systems, LLC 545 WEST 500 SOUTH SUITE 100 Bountiful, UT 84010 |
Contact | Bret M Berry |
Correspondent | Bret M Berry Reliance Medical Systems, LLC 545 South 500 West SUITE 100 Bountiful, UT 84010 |
Product Code | MNI |
Subsequent Product Code | KWP |
Subsequent Product Code | KWQ |
Subsequent Product Code | MNH |
CFR Regulation Number | 888.3070 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2015-07-31 |
Decision Date | 2015-09-17 |