The following data is part of a premarket notification filed by Precision Spine, Inc. with the FDA for Reform® Poct System.
Device ID | K162300 |
510k Number | K162300 |
Device Name: | Reform® POCT System |
Classification | Posterior Cervical Screw System |
Applicant | PRECISION SPINE, INC. 2050 EXECUTIVE DRIVE Pearl, MS 39208 |
Contact | Michael C. Dawson |
Correspondent | Kenneth C. Maxwell EMPIRICAL TESTING CORP. 4628 NORTHPARK DRIVE Colorado Springs, CO 80918 |
Product Code | NKG |
CFR Regulation Number | 888.3075 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2016-08-16 |
Decision Date | 2016-11-22 |
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 |