The following data is part of a premarket notification filed by Precision Spine, Inc. with the FDA for Reform® Midline Cortical Screw System.
| Device ID | K173130 |
| 510k Number | K173130 |
| Device Name: | Reform® Midline Cortical Screw System |
| Classification | Thoracolumbosacral Pedicle Screw System |
| Applicant | Precision Spine, Inc. 2050 Executive Drive Pearl, MS 39208 |
| Contact | Michael C. Dawson |
| Correspondent | Meredith L. May Empirical Technologies 4628 Northpark Drive Colorado Springs, CO 80918 |
| Product Code | NKB |
| CFR Regulation Number | 888.3070 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2017-09-29 |
| Decision Date | 2017-12-19 |
| Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() REFORM 98203546 not registered Live/Pending |
Loveland Products, Inc. 2023-09-29 |
![]() REFORM 98089366 not registered Live/Pending |
Loveland Products, Inc. 2023-07-18 |
![]() REFORM 98081488 not registered Live/Pending |
Winpak Ltd. 2023-07-12 |
![]() REFORM 97783633 not registered Live/Pending |
9376-1377 Québec inc. 2023-02-07 |
![]() REFORM 97661242 not registered Live/Pending |
Reform LLC 2022-11-03 |
![]() REFORM 97491288 not registered Live/Pending |
Baker Hughes Holdings LLC 2022-07-06 |
![]() REFORM 90844523 not registered Live/Pending |
Incase Designs Corp. 2021-07-23 |
![]() REFORM 90702763 not registered Live/Pending |
Reform Group Holdings ApS 2021-05-11 |
![]() REFORM 90702754 not registered Live/Pending |
Reform Group Holdings ApS 2021-05-11 |
![]() REFORM 90281099 not registered Live/Pending |
Criminal Justice Reform Foundation 2020-10-27 |
![]() REFORM 88933318 not registered Live/Pending |
Loveland Products, Inc. 2020-05-26 |
![]() REFORM 88668615 not registered Live/Pending |
Reform Unlimited 2019-10-25 |