Brigade

Brigade Plate Pin, 12mm Ø.080 Fixation

Registry build 21.09.26
14manufacturers in China registered for this device type
48catalogue numbers in this listing
21510(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 Brigade
Listed by Nuvasive, Inc., 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, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
510(k) K121837
Record published 2015-10-24
Record revised 2025-06-11 (version 11)

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

Catalogue Numbers

Catalogue numbers for Brigade
Catalogue number Size Status
7880034 In distribution
7806520 In distribution
7806525 In distribution
7805537 In distribution
1585332 In distribution
1567422 In distribution
7880040 In distribution
7805540 In distribution
7806540 In distribution
7880044 In distribution
7805535 In distribution
1585335 In distribution
7881036 In distribution
7806535 In distribution
7806527 In distribution
7805525 In distribution
1567428 In distribution
7805530 In distribution
7880046 In distribution
1577434 In distribution
7806522 In distribution
1567431 In distribution
1567423 In distribution
1567421 In distribution
1588862 In distribution
7880038 In distribution
7805522 In distribution
7880036 In distribution
1588861 In distribution
7881026 In distribution
7805532 In distribution
7881032 In distribution
1585333 In distribution
1567427 In distribution
1577432 In distribution
7880042 In distribution
1585334 In distribution
7805527 In distribution
7881034 In distribution
1567425 In distribution
7806532 In distribution
7881030 In distribution
7806537 In distribution
1585336 In distribution
7805520 In distribution
7806530 In distribution
7881028 In distribution
1567430 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
K131025 2013-11-27
K130868 2013-08-29
K122081 2013-02-01
K121815 2012-10-23
K121837 2012-07-16
K111866 2011-07-22
K111410 2011-06-20
K103750 2011-03-03
K093804 2010-02-19
K091071 2009-05-08
K083341 2009-03-20
K082070 2008-09-24
K073275 2008-01-29
K072339 2007-10-19
K071329 2007-08-08
K070148 2007-07-31
K070273 2007-04-03
K062590 2007-01-18
K061789 2006-08-10
K053581 2006-02-17
K041447 2004-08-16

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