Slim-LOC

SLIM-LOC ANTERIOR CERVICAL PLATE SYSTEM SCREW, SELF-DRILLING 4.5 x 17mm

Registry build 21.09.26
14manufacturers in China registered for this device type
21catalogue numbers in this listing
10510(k) clearances naming this product code
8recalls on this 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 Slim-LOC
Listed by Depuy 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 Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer
510(k) K013877
Record published 2015-09-24
Record revised 2025-07-02 (version 6)

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
Distribution end date 2019-04-30

Catalogue Numbers

Catalogue numbers for Slim-LOC
Catalogue number Size Status
179606116 In distribution
179607017 Withdrawn
179606112 Withdrawn
179606018 Withdrawn
179607014 Withdrawn
179606014 Withdrawn
179606013 Withdrawn
179607018 Withdrawn
179606020 Withdrawn
179606012 Withdrawn
179606022 Withdrawn
179606026 Withdrawn
179607013 Withdrawn
179607016 Withdrawn
179607015 Withdrawn
179606114 Withdrawn
179606017 Withdrawn
179606024 Withdrawn
179606015 Withdrawn
179606016 Withdrawn
179607012 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
K100070 2010-02-04
K082273 2008-09-10
K080191 2008-04-02
K072546 2007-10-05
K070994 2007-05-09
K052546 2006-02-03
K052552 2005-10-13
K042544 2004-11-23
K041205 2004-08-17
K040655 2004-06-02

Recalls

8 of these are Class II. Class II means a temporary or reversible health consequence. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity Closed
2016-10-12 Class II Under Investigation by firm SKYLINE Variable Ti screws may have contained SKYLINE Constrained Ti screws within the packaging. 1 unit 2017-09-18
2016-10-12 Class II Under Investigation by firm SKYLINE Variable Ti screws may have contained SKYLINE Constrained Ti screws within the packaging. 14 units 2017-09-18
2016-10-12 Class II Under Investigation by firm SKYLINE Variable Ti screws may have contained SKYLINE Constrained Ti screws within the packaging. 6 units 2017-09-18
2016-10-12 Class II Under Investigation by firm SKYLINE Variable Ti screws may have contained SKYLINE Constrained Ti screws within the packaging. 9 units 2017-09-18
2016-10-12 Class II Under Investigation by firm SKYLINE Variable Ti screws may have contained SKYLINE Constrained Ti screws within the packaging. 12 units 2017-09-18
2016-10-12 Class II Under Investigation by firm SKYLINE Variable Ti screws may have contained SKYLINE Constrained Ti screws within the packaging. 9 units 2017-09-18
2016-10-12 Class II Under Investigation by firm SKYLINE Variable Ti screws may have contained SKYLINE Constrained Ti screws within the packaging. 21 units 2017-09-18
2015-11-20 Class II Device Design Manufacturing error within the Torque Handle may prohibit some handles from being able to fully assemble with the tightener shaft. The design of the inspection gage does not account for the additional shift length 16 devices 2017-07-03

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