Locking Proximal Femur Plate System

120 Deg x 4.5mm Varus Plate, 14mm Offset, 5 Hole

Registry build 21.09.26
22manufacturers in China registered for this device type
69catalogue numbers in this listing
15510(k) clearances naming this product code
4recalls on this code

Who Else Makes It

Concentrated in Jiangsu (10), Shanghai (4), Zhejiang (3). 12 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code HRS
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
Stryker (Suzhou) Medical Technology Co., Ltd. Suzhou Jiangsu Contract manufacturer 19
Suzhou Kangli Orthopaedics Instrument Co., Ltd. Zhangjiagang Jiangsu Contract manufacturer 11
Kingj Medical Co., Ltd. Zhangjiagang Jiangsu Contract manufacturer 7
Hangzhou Sino-MIM Technology Co., Ltd. Hangzhou Zhejiang Contract manufacturer 6
Suzhou AND Science & Technology Development Corp. Zhangjiagang Jiangsu Contract manufacturer 5
Beijing AK Medical Co., Ltd. Changping District Beijing Contract manufacturer 3

Showing 12 of 22. All 22 manufacturers in China registered for Plate, Fixation, Bone

Record

Regulatory record for Locking Proximal Femur Plate System
Listed by Orthopediatrics, Corp, United States
FDA product code HRS
Device type Plate, Fixation, Bone
Device class Class 2
Regulation 21 CFR 888.3030
Establishment Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer
510(k) K111086
Record published 2015-08-01
Record revised 2024-02-19 (version 4)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Single use Yes
Prescription Prescription only
Label carries lot or batch number
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for Locking Proximal Femur Plate System
Catalogue number Size Status
00-0907-1143 In distribution
00-0907-1265 In distribution
00-0907-0143 In distribution
00-0907-2206 In distribution
00-0907-0182 In distribution
00-0907-1463 In distribution
00-0907-1324 In distribution
00-0907-2114 In distribution
00-0907-0104 In distribution
00-0907-4206 In distribution
00-0907-2204 In distribution
00-0907-2209 In distribution
00-0907-2108 In distribution
00-0907-1164 In distribution
00-0907-4105 In distribution
00-0907-1464 In distribution
00-0907-1404 In distribution
00-0907-2210 In distribution
00-0907-2208 In distribution
00-0907-0142 In distribution
00-0907-1203 In distribution
00-0907-3103 In distribution
00-0907-0183 In distribution
00-0907-1303 In distribution
00-0907-2109 In distribution
00-0907-1465 In distribution
00-0907-1424 In distribution
00-0907-2106 In distribution
00-0907-2105 In distribution
00-0907-1263 In distribution
00-0907-1344 In distribution
00-0907-0144 In distribution
00-0907-3203 In distribution
00-0907-2104 In distribution
00-0907-1165 In distribution
00-0907-1304 In distribution
00-0907-4205 In distribution
00-0907-0184 In distribution
00-0907-4106 In distribution
00-0907-2107 In distribution
00-0907-2203 In distribution
00-0907-1243 In distribution
00-0907-2112 In distribution
00-0907-2207 In distribution
00-0907-1363 In distribution
00-0907-2103 In distribution
00-0907-1444 In distribution
00-0907-2205 In distribution
00-0907-2216 In distribution
00-0907-3205 In distribution
00-0907-1365 In distribution
00-0907-2111 In distribution
00-0907-4103 In distribution
00-0907-4104 In distribution
00-0907-3105 In distribution
00-0907-1403 In distribution
00-0907-2110 In distribution
00-0907-0103 In distribution
00-0907-1364 In distribution
00-0907-2214 In distribution
00-0907-0102 In distribution
00-0907-1163 In distribution
00-0907-2116 In distribution
00-0907-1123 In distribution
00-0907-2212 In distribution
00-0907-2211 In distribution
00-0907-4203 In distribution
00-0907-1264 In distribution
00-0907-1223 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Pectus System Biomet Microfixation 4,662
Arthrex® Arthrex, Inc. 3,031
Evos Smith & Nephew, Inc. 2,235
Peri-Loc Smith & Nephew, Inc. 2,196
OsteoMed Osteomed 1,961
VariAx Stryker GmbH 1,934
Aptus Medartis Inc. 1,688
TC-100 Smith & Nephew, Inc. 1,639
Plate, Fixation, Bone Synthes Gmbh 1,613
Anthem Globus Medical, Inc. 1,551
Acumed Acumed LLC 1,360
Signex Osteonic Co., Ltd. 1,310

Showing 12 of 3,530. All products under Plate, Fixation, Bone

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K260323 2026-04-30
K252600 2025-10-09
K243963 2025-04-29
K190992 2019-08-06
K172425 2017-12-06
K171173 2017-08-24
K162307 2016-09-27
K140431 2014-07-29
K110959 2011-08-05
K111086 2011-06-17
K100240 2010-05-17
K090666 2009-04-24
K083286 2009-01-30
K081407 2008-07-22
K073344 2008-02-19

Recalls Naming This Product

1 recall names this product by its own identifier, the 510(k) it is cleared under.

Recalls naming the identifiers of Locking Proximal Femur Plate System
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Orthopediatrics, Corp 510(k) number 2015-07-28 Class II Packaging process control The 00-0903-2510, 3.5mm x 10mm Non Locking Cortical Screw, Lot # 150192-J package may contain a different screw. The screw in the package is a 00-0903-2526, 3.5mm x 26mm, and is etched correctly. 5 2016-03-17

Recalls

3 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
2013-09-26 Class II Labeling mix-ups The firm identified, through complaints that the 3.5MM LOCKING SCREW packaging material was marked as a 3.5mm screw and the part number was correct but that the description indicated a 7.0mm screw. Upon investigation, it has been determined 7 units shipped 2013-12-26
2012-10-18 Class II Nonconforming Material/Component Complaint received from sales representative that the drill guide tubes would not screw into replenishment instrument. Upon investigation, it has been determined that the device was not manufactured to design specifications and will not fun 24 2013-09-18
2012-06-14 Class II Error in labeling The device is a Left 8 hole plate but is incorrectly labeled and etched as a Right device. 15 devices 2013-04-30

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