Presidio Anterior Lumbar Fixation System

Torque Limiting Straight Handle, 15in/lbs, 1/4 Sq.

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 Presidio Anterior Lumbar Fixation 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) K093200
Record published 2019-11-07
Record revised 2025-11-20 (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
Latex Contains natural rubber latex
Label carries lot or batch number
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for Presidio Anterior Lumbar Fixation System
Catalogue number Size Status
125-376 In distribution
125-372 In distribution
2016-0064 In distribution
125-365-35 In distribution
125-365-25 In distribution
125-609 In distribution
125-10-34 In distribution
125-455-30 In distribution
125-50-36 In distribution
125-355-35 In distribution
125-375 In distribution
114-124 In distribution
125-620 In distribution
125-455-20 In distribution
125-10-42 In distribution
125-604 In distribution
114-126 In distribution
125-606 In distribution
125-625 In distribution
125-10-44 In distribution
125-097 In distribution
125-10-46 In distribution
125-655-20 In distribution
125-605 In distribution
125-50-38 In distribution
125-655-25 In distribution
125-10-32 In distribution
125-371 In distribution
125-50-44 In distribution
161-4-040 In distribution
125-655-40 In distribution
125-378 In distribution
125-455-40 In distribution
112-215 In distribution
125-10-36 In distribution
125-374 In distribution
2014-0137 In distribution
125-377 In distribution
125-355-20 In distribution
125-50-42 In distribution
125-355-25 In distribution
125-10-40 In distribution
125-611 In distribution
125-655-30 In distribution
125-455-25 In distribution
125-355-18 In distribution
125-603 In distribution
125-50-46 In distribution
125-370 In distribution
125-365-30 In distribution
125-188 In distribution
125-50-34 In distribution
125-365-20 In distribution
125-607 In distribution
125-608 In distribution
125-610 In distribution
125-373 In distribution
125-354 In distribution
125-455-35 In distribution
125-600 In distribution
2016-0183 In distribution
125-599 In distribution
125-355-40 In distribution
125-50-32 In distribution
125-544 In distribution
125-619 In distribution
125-355-30 In distribution
125-601 In distribution
125-612 In distribution
125-194 In distribution
125-655-35 In distribution
125-618 In distribution
2016-0063 In distribution
125-365-40 In distribution
114-527 In distribution
125-545 In distribution
125-633 In distribution
125-10-38 In distribution
125-50-40 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