ABC

ABC Self-Locking Revision Screw 4.5X17MM

Registry build 21.09.26
14manufacturers in China registered for this device type
92catalogue numbers in this listing
11510(k) clearances naming this product code
1recall

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 ABC
Listed by Aesculap AG, Germany
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, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
Record published 2015-09-24
Record revised 2025-11-20 (version 16)

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 2025-10-28

Catalogue Numbers

Catalogue numbers for ABC
Catalogue number Size Status
FJ783T Height : 2.950 MM Withdrawn
FJ802T Diameter (mm) : 4.000 MM Withdrawn
FJ805T Length : 25.000 MM Withdrawn
FJ943T Diameter (mm) : 4.500 MM Withdrawn
FJ873T Withdrawn
FJ933T Length : 16.000 MM Withdrawn
FJ751T Height : 2.950 MM Withdrawn
FJ764T Height : 2.950 MM Withdrawn
FJ752T Height : 2.950 MM Withdrawn
FJ772T Height : 2.950 MM Withdrawn
FJ881T Withdrawn
FJ803T Diameter (mm) : 4.000 MM Withdrawn
FJ797T Diameter (mm) : 4.000 MM Withdrawn
FJ740T Height : 2.950 MM Withdrawn
FJ818T Length : 18.000 MM Withdrawn
FJ776T Height : 2.950 MM Withdrawn
FJ880T Withdrawn
FJ770T Height : 2.950 MM Withdrawn
FJ851T Length : 13.000 MM Withdrawn
FJ792T Diameter (mm) : 4.000 MM Withdrawn
FJ771T Height : 2.950 MM Withdrawn
FJ748T Height : 2.950 MM Withdrawn
FJ791T Length : 11.000 MM Withdrawn
FJ796T Diameter (mm) : 4.000 MM Withdrawn
FJ787T Height : 2.950 MM Withdrawn
FJ758T Height : 2.950 MM Withdrawn
FJ865T Withdrawn
FJ807T Diameter (mm) : 4.000 MM Withdrawn
FJ872T Withdrawn
FJ795T Length : 15.000 MM Withdrawn
FJ780T Height : 2.950 MM Withdrawn
FJ789T Height : 2.950 MM Withdrawn
FJ782T Height : 2.950 MM Withdrawn
FJ777T Height : 2.950 MM Withdrawn
FJ930T Diameter (mm) : 4.000 MM Withdrawn
FJ806T Diameter (mm) : 4.000 MM Withdrawn
FJ860T Withdrawn
FJ862T Withdrawn
FJ749T Height : 2.950 MM Withdrawn
FJ769T Height : 2.950 MM Withdrawn
FJ755T Height : 2.950 MM Withdrawn
FJ790T Length : 10.000 MM Withdrawn
FJ853T Length : 17.000 MM Withdrawn
FJ788T Height : 2.950 MM Withdrawn
FJ810T Diameter (mm) : 4.000 MM Withdrawn
FJ941T Length : 13.000 MM Withdrawn
FJ759T Height : 2.950 MM Withdrawn
FJ871T Withdrawn
FJ932T Length : 14.000 MM Withdrawn
FJ785T Height : 2.950 MM Withdrawn
FJ816T Diameter (mm) : 4.000 MM Withdrawn
FJ877T Withdrawn
FJ867T Withdrawn
FJ931T Diameter (mm) : 4.000 MM Withdrawn
FJ765T Height : 2.950 MM Withdrawn
FJ861T Withdrawn
FJ801T Length : 21.000 MM Withdrawn
FJ878T Withdrawn
FJ741T Height : 2.950 MM Withdrawn
FJ778T Height : 2.950 MM Withdrawn
FJ760T Height : 2.950 MM Withdrawn
FJ808T Diameter (mm) : 4.000 MM Withdrawn
FJ768T Height : 2.950 MM Withdrawn
FJ774T Height : 2.950 MM Withdrawn
FJ812T Diameter (mm) : 4.000 MM Withdrawn
FJ852T Length : 15.000 MM Withdrawn
FJ942T Length : 15.000 MM Withdrawn
FJ750T Height : 2.950 MM Withdrawn
FJ762T Height : 2.950 MM Withdrawn
FJ781T Height : 2.950 MM Withdrawn
FJ799T Length : 19.000 MM Withdrawn
FJ879T Withdrawn
FJ786T Height : 2.950 MM Withdrawn
FJ870T Withdrawn
FJ814T Length : 14.000 MM Withdrawn
FJ800T Length : 20.000 MM Withdrawn
FJ804T Length : 24.000 MM Withdrawn
FJ779T Height : 2.950 MM Withdrawn
FJ754T Height : 2.950 MM Withdrawn
FJ761T Height : 2.950 MM Withdrawn
FJ866T Withdrawn
FJ744T Height : 2.950 MM Withdrawn
FJ798T Length : 18.000 MM Withdrawn
FJ934T Length : 18.000 MM Withdrawn
FJ773T Height : 2.950 MM Withdrawn
FJ793T Length : 13.000 MM Withdrawn
FJ794T Diameter (mm) : 4.000 MM Withdrawn
FJ753T Height : 2.950 MM Withdrawn
FJ784T Height : 2.950 MM Withdrawn
FJ742T Height : 2.950 MM Withdrawn
FJ743T Height : 2.950 MM Withdrawn
FJ763T Height : 2.950 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
K050813 2005-05-04
K050804 2005-04-11
K040017 2004-05-14
K032059 2003-07-25
K011556 2001-11-16
K002824 2001-05-08
K000486 2000-04-14
K974706 1998-03-13
K953720 1995-11-02
K936269 1994-08-15
K913730 1992-03-12

Recalls

The FDA has not published a severity grade for these. 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
2012-01-24 Not classified Nonconforming Material/Component The firm has received complaints that the locking ring that sits in the head of the screw can come out of the screw head when engaged with the screwdriver if the screwdriver is improperly angled. 891 2012-12-13

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