Cannulated Screws

4.0mm CANNULATED SCREW 26mm LENGTH-TITANIUM

Registry build 21.09.26
17manufacturers in China registered for this device type
24catalogue numbers in this listing
16510(k) clearances naming this product code

Who Else Makes It

Concentrated in Jiangsu (6), Shanghai (4), Zhejiang (3). 13 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code KTT
Manufacturer City Province Registered as Device types
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
Canwell Medical Co., Ltd. Jinhua Zhejiang Contract manufacturer 42
Suzhou Elite Precision Machinery Co., Ltd. Kunshan Jiangsu Contract manufacturer 35
LX Precision Shanghai Co Ltd Shanghai Shanghai Contract manufacturer 19
Suzhou Ahno Medical Devices Co., Ltd. Suzhou Jiangsu Contract manufacturer 17
Turnxon Precision Co., Ltd. Dongguan Guangdong Contract manufacturer 17
Zibo Dante Co., Ltd. Zibo Shandong Contract manufacturer 17
Stryker Orthmed (Changzhou) Medical Instrument Co., Ltd. Changzhou Jiangsu Contract manufacturer 10
Hangzhou Sino-MIM Technology Co., Ltd. Hangzhou Zhejiang Contract manufacturer 6
Suzhou AND Science & Technology Development Corp. Zhangjiagang Jiangsu Contract manufacturer 5

Showing 12 of 17. All 17 manufacturers in China registered for Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component

Record

Regulatory record for Cannulated Screws
Listed by Smith & Nephew, Inc., United States
FDA product code KTT
Device type Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component
Device class Class 2
Regulation 21 CFR 888.3030
Establishment Contract manufacturer, Remanufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
510(k) K210837
Record published 2015-08-25
Record revised 2024-02-19 (version 7)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for Cannulated Screws
Catalogue number Size Status
71101026 In distribution
71101040 In distribution
71101028 In distribution
71101046 In distribution
71101042 In distribution
71101065 In distribution
71101056 In distribution
71101054 In distribution
71101022 In distribution
71101020 In distribution
71101048 In distribution
71101070 In distribution
71101030 In distribution
71101036 In distribution
71101034 In distribution
71101050 In distribution
71101024 In distribution
71101058 In distribution
71101060 In distribution
71101038 In distribution
71101032 In distribution
71101052 In distribution
71101044 In distribution
71119007 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Smart Correction Wishbone Medical Inc. 1,534
Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component Synthes Gmbh 880
LCP Synthes Gmbh 355
Orthex External Fixation System Orthopediatrics, Corp 353
Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component Sterilmed, Inc. 325
CHS Smith & Nephew, Inc. 321
Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component Stryker Sustainability Solutions 277
Hoffmann Stryker GmbH 239
Orthex Orthopediatrics, Corp 231
Orthex Vilex IN Tennessee, Inc. 221
Omega Stryker GmbH 212
eZ-Fix Orthopediatrics, Corp 207

Showing 12 of 530. All products under Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K210953 2021-07-29
K201253 2020-12-08
K202762 2020-11-16
K142520 2014-11-20
K130479 2013-05-14
K110069 2011-02-08
K093047 2010-09-27
K100795 2010-09-02
K092002 2009-12-10
K090926 2009-06-08
K072212 2008-03-07
K050849 2005-05-04
K042436 2004-10-07
K042312 2004-09-24
K031181 2003-07-14
K993289 1999-12-20

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