Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component

4.5MM 90 DEG TI Cann LC-Angled Blade Plate 12 HOLES/40MM-STE

Registry build 21.09.26
17manufacturers in China registered for this device type
146catalogue numbers in this listing

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 Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component
Listed by Synthes (U.S.A.) LP
FDA product code KTT
Device type Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component
Device class Class 2
Regulation 21 CFR 888.3030
510(k) K974537
Record published 2015-09-14
Record revised 2026-06-30 (version 9)

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
Distribution end date 2026-06-30

Catalogue Numbers

Catalogue numbers for Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component
Catalogue number Size Status
237.145S Withdrawn
414.226 Withdrawn
414.024 Withdrawn
414.250 Withdrawn
413.414 Withdrawn
437.124S Withdrawn
237.043S Withdrawn
412.252 Withdrawn
412.251 Withdrawn
414.295 Withdrawn
437.145S Withdrawn
SD311.204 Withdrawn
212.264 Withdrawn
212.266 Withdrawn
237.083S Withdrawn
413.435 Withdrawn
237.085S Withdrawn
413.490 Withdrawn
414.240 Withdrawn
393.71 Withdrawn
412.267 Withdrawn
212.265 Withdrawn
413.460 Withdrawn
437.084S Withdrawn
412.261 Withdrawn
212.267 Withdrawn
413.480 Withdrawn
393.54 Withdrawn
413.470 Withdrawn
SD311.202 Withdrawn
412.253 Withdrawn
212.260 Withdrawn
414.036 Withdrawn
437.083S Withdrawn
437.053S Withdrawn
414.115 Withdrawn
437.063S Withdrawn
437.104S Withdrawn
413.485 Withdrawn
414.046 Withdrawn
213.490 Withdrawn
412.264 Withdrawn
413.450 Withdrawn
437.043S Withdrawn
237.123S Withdrawn
237.053S Withdrawn
437.086S Withdrawn
212.263 Withdrawn
412.259 Withdrawn
237.126S Withdrawn
395.77 Withdrawn
437.143S Withdrawn
212.259 Withdrawn
414.070 Withdrawn
437.106S Withdrawn
237.105S Withdrawn
413.465 Withdrawn
414.276 Withdrawn
237.064S Withdrawn
414.264 Withdrawn
413.430 Withdrawn
414.236 Withdrawn
214.228 Withdrawn
412.263 Withdrawn
437.044S Withdrawn
414.140 Withdrawn
213.422 Withdrawn
414.100 Withdrawn
237.103S Withdrawn
414.258 Withdrawn
214.246 Withdrawn
212.254 Withdrawn
237.086S Withdrawn
414.125 Withdrawn
393.75 Withdrawn
412.254 Withdrawn
237.063S Withdrawn
212.262 Withdrawn
214.280 Withdrawn
413.440 Withdrawn
437.105S Withdrawn
414.068 Withdrawn
212.258 Withdrawn
237.084S Withdrawn
237.104S Withdrawn
414.290 Withdrawn
212.261 Withdrawn
414.080 Withdrawn
437.146S Withdrawn
213.414 Withdrawn
214.300 Withdrawn
395.693 Withdrawn
437.125S Withdrawn
414.020 Withdrawn
413.418 Withdrawn
237.054S Withdrawn
414.066 Withdrawn
413.445 Withdrawn
214.234 Withdrawn
414.030 Withdrawn
437.123S Withdrawn
237.144S Withdrawn
237.124S Withdrawn
437.085S Withdrawn
412.256 Withdrawn
412.260 Withdrawn
237.146S Withdrawn
395.70 Withdrawn
212.257 Withdrawn
413.455 Withdrawn
437.126S Withdrawn
212.252 Withdrawn
414.090 Withdrawn
214.250 Withdrawn
437.054S Withdrawn
212.255 Withdrawn
237.106S Withdrawn
437.103S Withdrawn
414.038 Withdrawn
412.255 Withdrawn
SD311.205 Withdrawn
212.253 Withdrawn
237.044S Withdrawn
437.144S Withdrawn
412.258 Withdrawn
412.257 Withdrawn
395.74 Withdrawn
212.256 Withdrawn
SD311.203 Withdrawn
414.076 Withdrawn
214.222 Withdrawn
213.430 Withdrawn
237.125S Withdrawn
395.692 Withdrawn
412.262 Withdrawn
412.265 Withdrawn
414.095 Withdrawn
395.73 Withdrawn
412.266 Withdrawn
237.143S Withdrawn
437.064S Withdrawn
213.460 Withdrawn
212.251 Withdrawn
413.475 Withdrawn
214.226 Withdrawn
413.422 Withdrawn

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

Recalls Naming This Product

3 recalls name this product by its own identifiers, the 510(k) it is cleared under.

Recalls naming the identifiers of Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Synthes (USA) Products LLC 510(k) number 2015-07-29 Class II Labeling design Labeling changes were made related to MR conditions that align with standard definitions for MR Safe, MR Conditional, and MR Unsafe. This recall identifies additional Trauma External Fixation System part numbers that should be considered MR 5306080 2016-09-27
Synthes Gmbh 510(k) number 2014-04-10 Class II Labeling Change Control Labeling changes have been made related to MR (Magnetic Resonance imaging) conditions as a result of changes in required protocols to designate a product MR Safe, MR Conditional, or MR Unsafe. 5,114,052 2016-08-26
Synthes Spine 510(k) number 2009-02-09 Not classified Process control Numbers are etched incorrectly on the product. 1,137 units 2009-12-15

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