NEO / Kinetic Anterior Cervical Plate System

Kinetic Single-Barrel Clip-On Fixed Angle Drill Guide

Registry build 21.09.26
14manufacturers in China registered for this device type
79catalogue numbers in this listing
14510(k) clearances naming this product code

Who Else Makes It

Concentrated in Jiangsu (5), Shanghai (3), Zhejiang (2). 8 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code KWQ
Manufacturer City Province Registered as Device types
Zhejiang Biomet Medical Products Co., Ltd. Jinhua Zhejiang Contract manufacturer 74
Apex (Guangzhou) Tools & Orthopedics Company Guangzhou Guangdong Contract manufacturer 62
Changzhou Biomet Medical Devices Co., Ltd. Changzhou Jiangsu Contract manufacturer 54
Paragon Medical Device (Changzhou) Co., Ltd. Changzhou Jiangsu Contract manufacturer 53
Shandong Weigao Orthopaedic Device Co., Ltd. Weihai Shandong Contract manufacturer 42
LX Precision Shanghai Co Ltd Shanghai Shanghai Contract manufacturer 19
APS Materials Suzhou Suzhou Jiangsu Contract manufacturer 18
Zibo Dante Co., Ltd. Zibo Shandong Contract manufacturer 17
Shanghai JPY ION-Tech Co., Ltd. Shanghai Shanghai Contract manufacturer 70
Medtronic (Changzhou) Medical Devices Technology Co., Ltd. Changzhou Jiangsu Manufacturer 53
Johnson & Johnson Medical (Depuy – Suzhou) Ltd. Suzhou Jiangsu Manufacturer 34
Double Medical Technology Inc. Xiamen Fujian Contract manufacturer 14

Showing 12 of 14. All 14 manufacturers in China registered for Appliance, Fixation, Spinal Intervertebral Body

Record

Regulatory record for NEO / Kinetic Anterior Cervical Plate System
Listed by Life Spine, United States
FDA product code KWQ
Device type Appliance, Fixation, Spinal Intervertebral Body
Device class Class 2
Regulation 21 CFR 888.3060
Establishment Specification developer, Manufacturer
510(k) K062643
Record published 2019-11-07
Record revised 2024-09-11 (version 5)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Single use Yes
Prescription Prescription only
Label carries lot or batch number
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for NEO / Kinetic Anterior Cervical Plate System
Catalogue number Size Status
116-320 In distribution
101-014 In distribution
201-014 In distribution
203-012 In distribution
2014-0141 In distribution
103-014 In distribution
202-010 In distribution
113-203 In distribution
113-105-2 In distribution
2009-0025 In distribution
2008-0045-02 In distribution
201-016 In distribution
2010-0014 In distribution
203-014 In distribution
1502-044 In distribution
201-010 In distribution
202-018 In distribution
113-136 In distribution
103-016 In distribution
2017-0120 In distribution
103-010 In distribution
111-001 In distribution
113-230 In distribution
114-012 In distribution
116-221 In distribution
113-297 In distribution
113-950-3 In distribution
2009-0064 In distribution
114-203 In distribution
113-232 In distribution
113-204 In distribution
103-018 In distribution
113-234-1 In distribution
102-014 In distribution
101-012 In distribution
202-014 In distribution
101-016 In distribution
113-052 In distribution
113-126 In distribution
2018-0080 In distribution
113-013 In distribution
102-018 In distribution
102-016 In distribution
113-050 In distribution
113-234-2 In distribution
116-222 In distribution
101-010 In distribution
203-016 In distribution
113-124 In distribution
201-012 In distribution
102-010 In distribution
113-105 In distribution
113-831 In distribution
102-012 In distribution
113-130 In distribution
2008-0031-02 In distribution
113-1000 In distribution
2008-0046-02 In distribution
114-002 In distribution
114-003 In distribution
2016-0095 In distribution
203-010 In distribution
101-018 In distribution
2013-0113 In distribution
113-128 In distribution
113-012 In distribution
113-141 In distribution
202-012 In distribution
203-018 In distribution
2018-0082 In distribution
113-982 In distribution
113-007 In distribution
201-018 In distribution
2009-0070 In distribution
103-012 In distribution
113-983 In distribution
113-231 In distribution
2009-0062 In distribution
202-016 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
ReLine Nuvasive, Inc. 2,998
CD Horizon® Spinal System Medtronic Sofamor Danek, Inc. 2,568
Creo Globus Medical, Inc. 1,765
AccelFix Spinal Fixation System L&K Biomed Co., Ltd. 1,755
Ozark Cervical Plate System VB Spine LLC 1,460
Sirion Astura Medical 1,246
Apex Spine System Spinecraft LLC 1,187
AnyPlus Spinal Fixation System GS Medical Co., Ltd. 986
Astra Spine System Spinecraft LLC 970
Zavation Zavation 966
ACP Nuvasive, Inc. 918
Polaris™ 5.5 Spinal System Biomet Spine 877

Showing 12 of 855. All products under Appliance, Fixation, Spinal Intervertebral Body

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K243369 2024-12-11
K222628 2022-11-16
K180166 2018-06-22
K172131 2017-08-28
K152282 2015-11-20
K132589 2013-10-08
K130202 2013-04-29
K103423 2011-06-01
K093200 2010-01-19
K073479 2008-01-09
K070285 2007-03-13
K062643 2006-11-16
K062831 2006-10-19
K040844 2004-07-23

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer