CD Horizon™ ModuLeX™ FNS Screw Set

Shank 55901526560 CAN OG FNS 6.5X60 TI S

Registry build 21.09.26
14manufacturers in China registered for this device type
33catalogue numbers in this listing
20510(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 CD Horizon™ ModuLeX™ FNS Screw Set
Listed by Medtronic Sofamor Danek, Inc., United States
FDA product code KWQ
Device type Appliance, Fixation, Spinal Intervertebral Body
Device class Class 2
Regulation 21 CFR 888.3060
510(k) K232141
Record published 2024-12-29

Specifications

Specifications
MRI safety MR Conditional
Sterilisation Moist Heat or Steam Sterilization
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for CD Horizon™ ModuLeX™ FNS Screw Set
Catalogue number Size Per pack Status
55900525545 In distribution
55901526560 In distribution
55901529535 In distribution
55901526540 In distribution
55901521560 In distribution
55901525555 In distribution
55902526550 2 In distribution
55902527540 2 In distribution
55901524535 In distribution
55901527535 In distribution
55902527545 2 In distribution
55902525540 2 In distribution
55902526545 2 In distribution
55901528550 In distribution
55901524560 In distribution
55900526550 In distribution
55901524545 In distribution
55900528550 In distribution
55902528545 2 In distribution
55901529555 In distribution
55901527540 In distribution
55902526555 2 In distribution
55901529540 In distribution
55901524550 In distribution
55902527550 2 In distribution
55901529565 In distribution
55901528535 In distribution
55901526530 In distribution
55901527560 In distribution
55900524545 In distribution
55902524545 2 In distribution
55900526545 In distribution
55902525535 2 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
K140417 2014-07-09
K081038 2008-08-15
K063100 2007-02-23
K061274 2006-05-25
K050117 2005-02-17
K043151 2005-02-01
K031782 2005-02-01
K042922 2004-11-19
K042499 2004-10-07
K042235 2004-09-17
K042025 2004-08-25
K041217 2004-05-28
K040962 2004-05-14
K032265 2003-08-11
K030327 2003-02-26
K021761 2002-09-17
K021461 2002-07-22
K021226 2002-05-13
K013665 2002-01-29
K994239 2000-06-19

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