The following data is part of a premarket notification filed by Precision Spine, Inc. with the FDA for Reform Pedicle Screw System.
Device ID | K150856 |
510k Number | K150856 |
Device Name: | Reform Pedicle Screw System |
Classification | Thoracolumbosacral Pedicle Screw System |
Applicant | PRECISION SPINE, INC. 2050 EXECUTIVE DRIVE Pearl, MS 39208 |
Contact | Michael Dawson |
Correspondent | Kenneth C Maxwell EMPIRICAL CONSULTING, LLC 4628 NORTHPARK DRIVE Colorado Springs, CO 80918 |
Product Code | NKB |
Subsequent Product Code | KWP |
Subsequent Product Code | MNH |
Subsequent Product Code | MNI |
Subsequent Product Code | OSH |
CFR Regulation Number | 888.3070 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2015-03-31 |
Decision Date | 2015-07-07 |
Summary: | summary |