Spartan Hip Stem

63 catalogue numbers from 111-44-1104, listed by Signature Orthopaedics PTY Limited, Australia, under Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate. 14 manufacturers in China are registered for this product code.

Registry build 21.09.26
14manufacturers in China registered for this device type
63catalogue numbers in this listing
8510(k) clearances naming this product code
2recalls on this code

Who Else Makes It

Concentrated in Jiangsu (8), Shanghai (2), 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 MEH
Manufacturer City Province Registered as Device types
Canwell Medical Co., Ltd. Jinhua Zhejiang Contract manufacturer 42
Suzhou Elite Precision Machinery Co., Ltd. Kunshan Jiangsu Contract manufacturer 35
B-ONE Medical (Suzhou) Co., Ltd. Suzhou Jiangsu Contract manufacturer 23
Stryker (Suzhou) Medical Technology Co., Ltd. Suzhou Jiangsu Contract manufacturer 19
APS Materials Suzhou Suzhou Jiangsu Contract manufacturer 18
Xian Airfoil Technology Co., Ltd. Xian Shaanxi Contract manufacturer 8
Lincotek (Wuxi) Co., Ltd. Wuxi Jiangsu Contract manufacturer 7
b-ONE Medical (Beijing) Co., Ltd. Beijing Beijing Contract manufacturer 7
Zimmer (Shanghai) Medical International Trading Co., Ltd. Shanghai Shanghai Exporter 106
Zhejiang Biomet Medical Products Co., Ltd. Jinhua Zhejiang Contract manufacturer 74
Shanghai JPY ION-Tech Co., Ltd. Shanghai Shanghai Contract manufacturer 70
Changzhou Biomet Medical Devices Co., Ltd. Changzhou Jiangsu Contract manufacturer 54

Showing 12 of 14. All 14 manufacturers in China registered for Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate

Record

Regulatory record for Spartan Hip Stem
Listed by Signature Orthopaedics PTY Limited, Australia
FDA product code MEH
Device type Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate
Device class Class 2
Regulation 21 CFR 888.3353
Establishment Contract manufacturer, Specification developer, Complaint-file establishment, Manufacturer
510(k) K192883
Record published 2020-09-01

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date, manufacturing date

Catalogue Numbers

Catalogue numbers for Spartan Hip Stem
Catalogue number Size Status
111-44-1104 In distribution
111-44-0007 In distribution
111-44-0107 In distribution
111-44-1203 In distribution
111-44-1212 In distribution
111-44-0208 In distribution
111-44-1005 In distribution
111-44-1011 In distribution
111-44-1108 In distribution
111-44-0005 In distribution
111-44-1211 In distribution
111-44-1002 In distribution
111-44-1111 In distribution
111-44-1102 In distribution
111-44-0011 In distribution
111-44-1007 In distribution
111-44-0004 In distribution
111-44-0003 In distribution
111-44-1210 In distribution
111-44-1008 In distribution
111-44-1107 In distribution
111-44-0009 In distribution
111-44-1003 In distribution
111-44-0103 In distribution
111-44-1205 In distribution
111-44-0105 In distribution
111-44-0209 In distribution
111-44-1105 In distribution
111-44-1010 In distribution
111-44-0010 In distribution
111-44-1204 In distribution
111-44-0008 In distribution
111-44-0109 In distribution
111-44-0111 In distribution
111-44-1209 In distribution
111-44-0104 In distribution
111-44-0108 In distribution
111-44-1112 In distribution
111-44-0207 In distribution
111-44-1004 In distribution
111-44-0205 In distribution
111-44-0211 In distribution
111-44-1106 In distribution
111-44-1208 In distribution
111-44-1202 In distribution
111-44-0210 In distribution
111-44-0206 In distribution
111-44-0203 In distribution
111-44-1109 In distribution
111-44-1206 In distribution
111-44-0212 In distribution
111-44-1009 In distribution
111-44-1207 In distribution
111-44-1012 In distribution
111-44-1110 In distribution
111-44-1006 In distribution
111-44-0110 In distribution
111-44-0204 In distribution
111-44-0012 In distribution
111-44-0106 In distribution
111-44-0006 In distribution
111-44-1103 In distribution
111-44-0112 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Alteon Exactech, Inc. 326
Novation Exactech, Inc. 317
Pinnacle Depuy Orthopaedics, Inc. 305
SP-CL Hip Stem Waldemar Link GmbH & Co. KG 219
Emperion Smith & Nephew, Inc. 201
MobileLink Acetabular Cup System Waldemar Link GmbH & Co. KG 154
Instrument Howmedica Osteonics Corp 145
Restoration Howmedica Osteonics Corp 144
Mfinity Femoral System Medacta International SA 138
Echelon Smith & Nephew, Inc. 134
Trinity Acetabular Hip System Corin Limited 128
Redapt Smith & Nephew, Inc. 127

Showing 12 of 805. All products under Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K243162 2024-11-25
K241690 2024-08-01
K220495 2023-01-13
K211742 2022-01-07
K211505 2021-09-24
K201278 2020-09-21
K161155 2016-07-19
K153131 2016-06-03

Recalls

2 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
2021-04-20 Class II Labeling mix-ups Product mislabeled, with the incorrect product inside the package. 3 units 2023-01-19
2018-02-02 Class II Labeling mix-ups This recall has been identified due to the batch being mislabeled, with the packaged
component’s size not corresponding to the label. Therefore, the product intended to be used
for the procedure may not be included in the packaging resultin
10 2018-08-08

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