ShurFit Interbody Device

Wide PLIF Cage Peek 15 degree 25 x 10 x 13mm

Registry build 21.09.26
14manufacturers in China registered for this device type
109catalogue numbers in this listing
4510(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 ShurFit Interbody Device
Listed by Precision Spine, Inc., United States
FDA product code KWQ
Device type Appliance, Fixation, Spinal Intervertebral Body
Device class Class 2
Regulation 21 CFR 888.3060
Establishment Manufacturer
510(k) K092193
Record published 2019-04-29
Record revised 2025-07-14 (version 4)

Specifications

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

Catalogue Numbers

Catalogue numbers for ShurFit Interbody Device
Catalogue number Size Status
26-250815-16 In distribution
26-251000-14 In distribution
26-250810-14 In distribution
26-221000-08 In distribution
26-220810-16 In distribution
26-220815-12 In distribution
21-1026 In distribution
26-251015-13 In distribution
26-251005-10 In distribution
26-250810-10 In distribution
26-250800-11 In distribution
44-3010-12 In distribution
TLIF30-16P In distribution
ALIF0832-11P In distribution
TLIF24-12P In distribution
26-221000-09 In distribution
ALIF0839-21P In distribution
44-3515-14 In distribution
26-251000-08 In distribution
26-251005-11 In distribution
TLIF30-08 In distribution
68-SC-0200 In distribution
26-221000-10 In distribution
26-220805-15 In distribution
44-3005-08 In distribution
26-251000-13 In distribution
26-251000-12 In distribution
26-221005-14 In distribution
26-221005-12 In distribution
26-251010-13 In distribution
07-2910 In distribution
26-250805-14 In distribution
PLIF22-08P In distribution
21-1039 In distribution
TLIF30-06P In distribution
PLIF25-11P In distribution
26-220805-14 In distribution
26-221000-07 In distribution
26-251005-13 In distribution
26-251000-09 In distribution
21-1005 In distribution
26-220800-08 In distribution
26-251010-10 In distribution
PLIF22-09P In distribution
21-1001-CD In distribution
26-251015-16 In distribution
38-2914 In distribution
26-250815-12 In distribution
26-251015-10 In distribution
PLIF22-12P In distribution
26-251000-10 In distribution
26-221010-15 In distribution
TLIF30-14P In distribution
PLIF25-10P In distribution
26-251015-14 In distribution
44-2510-10 In distribution
TLIF30-11P In distribution
44-2515-10 In distribution
44-2505-14 In distribution
26-250815-13 In distribution
26-251015-11 In distribution
26-221010-09 In distribution
44-3510-10 In distribution
26-220810-09 In distribution
21-1032 In distribution
26-220800-15 In distribution
PLIF22-10P In distribution
38-2916 In distribution
26-251005-14 In distribution
PLIF25-09P In distribution
07-2915 In distribution
26-221010-11 In distribution
49-BK-0100 In distribution
26-221010-10 In distribution
26-220815-10 In distribution
21-1006 In distribution
44-3005-10 In distribution
26-220810-10 In distribution
26-250805-09 In distribution
TLIF30-12 In distribution
44-2510-12 In distribution
21-1002-CD3 In distribution
26-221010-13 In distribution
26-251005-12 In distribution
26-220800-13 In distribution
ALIF1539-21P In distribution
26-220805-13 In distribution
26-221005-16 In distribution
26-250815-10 In distribution
38-2909 In distribution
26-221005-09 In distribution
26-251000-15 In distribution
26-221015-10 In distribution
26-251005-15 In distribution
38-2907 In distribution
26-221005-11 In distribution
26-221000-14 In distribution
26-251010-12 In distribution
26-221005-08 In distribution
26-250815-11 In distribution
26-220810-12 In distribution
26-251010-09 In distribution
26-251010-11 In distribution
26-221015-11 In distribution
44-1000 In distribution
21-1004 In distribution
26-250815-15 In distribution
TLIF24-07P In distribution
44-3005-14 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
K220324 2022-03-16
K212937 2021-11-04
K192494 2019-10-29
K162211 2016-11-28

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