XIA II

Thoracic Laminar Hook Large Offset, Right

Registry build 21.09.26
14manufacturers in China registered for this device type
44catalogue numbers in this listing
7510(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 XIA II
Listed by Stryker GmbH, Switzerland
FDA product code KWQ
Device type Appliance, Fixation, Spinal Intervertebral Body
Device class Class 2
Regulation 21 CFR 888.3060
Establishment Contract manufacturer, Specification developer, Complaint-file establishment, Manufacturer
Record published 2014-12-08
Record revised 2025-09-15 (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, manufacturing date
Sizes Length 25 to 100 mm
Distribution end date 2025-09-15

Catalogue Numbers

Catalogue numbers for XIA II
Catalogue number Size Status
03828645 Length 45.0 mm In distribution
03828760 Length 60.0 mm In distribution
03820555 Diameter: 5.5 Millimeter In distribution
03756230 In distribution
03821630 Length 30.0 mm In distribution
03828550 Length 50.0 mm In distribution
03821740 Length 40.0 mm In distribution
03821550 Diameter: 5.5 Millimeter In distribution
48218060 Length 60.0 mm In distribution
03828530 Diameter: 5.5 Millimeter In distribution
03828730 Length 30.0 mm In distribution
03821555 Diameter: 5.5 Millimeter In distribution
03828640 Length 40.0 mm In distribution
03821530 Diameter: 5.5 Millimeter In distribution
03829655 Length 55.0 mm In distribution
03821660 Diameter: 6.5 Millimeter In distribution
48218035 Diameter: 6.0 Millimeter In distribution
03820207 In distribution
03829645 Length 45.0 mm In distribution
48218090 Diameter: 6.0 Millimeter In distribution
03820208 In distribution
03829530 Length 30.0 mm In distribution
03828735 Length 35.0 mm In distribution
03802070 Length 70.0 mm In distribution
03821640 Diameter: 6.5 Millimeter In distribution
03820640 Diameter: 6.5 Millimeter In distribution
03821760 Length 60.0 mm Withdrawn
038215035 Length 35.0 mm Withdrawn
03829555 Diameter: 5.5 Millimeter Withdrawn
03821790 Diameter: 7.5 Millimeter Withdrawn
03820231 Withdrawn
03820242 Withdrawn
03827220 Withdrawn
03820680 Diameter: 6.5 Millimeter Withdrawn
03820214 Withdrawn
03820800 Length 100.0 mm Withdrawn
03820855 Diameter: 8.5 Millimeter Withdrawn
03820880 Length 80.0 mm Withdrawn
03820445 Diameter: 4.5 Millimeter Withdrawn
038204035 Length 35.0 mm Withdrawn
03805025 Length 25.0 mm Withdrawn
03805050 Diameter: 6.5 Millimeter Withdrawn
03821670 Length 70.0 mm Withdrawn
03820845 Length 45.0 mm Withdrawn

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
K221728 2022-10-19
K150700 2015-07-15
K150449 2015-03-20
K142237 2015-01-26
K142699 2014-12-31
K083020 2009-03-26
K083562 2009-03-25

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