AGC Tradition Knee System

95 catalogue numbers from 151075, listed by Biomet Orthopedics, United States, under Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer. 21 manufacturers in China are registered for this product code.

Registry build 21.09.26
21manufacturers in China registered for this device type
95catalogue numbers in this listing
2510(k) clearances naming this product code

Who Else Makes It

Concentrated in Jiangsu (10), Shanghai (4), Beijing (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 JWH
Manufacturer City Province Registered as Device types
MicroPort Orthopedics Global Supply Center Limited Shanghai Shanghai Contract manufacturer 82
Zhejiang Biomet Medical Products Co., Ltd. Jinhua Zhejiang Contract manufacturer 74
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
Guangzhou Aquila Precise Tools Limited Guangzhou Guangdong Contract manufacturer 28
B-ONE Medical (Suzhou) Co., Ltd. Suzhou Jiangsu Contract manufacturer 23
LX Precision Shanghai Co Ltd Shanghai Shanghai Contract manufacturer 19
Stryker (Suzhou) Medical Technology Co., Ltd. Suzhou Jiangsu Contract manufacturer 19
Stryker Orthmed (Changzhou) Medical Instrument Co., Ltd. Changzhou Jiangsu Contract manufacturer 10
b-ONE Medical (Beijing) Co., Ltd. Beijing Beijing Contract manufacturer 7
Changzhou Wastonortho Medical Appliance Co., Ltd. Changzhou Jiangsu Contract manufacturer 5

Showing 12 of 21. All 21 manufacturers in China registered for Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer

Record

Regulatory record for AGC Tradition Knee System
Listed by Biomet Orthopedics, United States
FDA product code JWH
Device type Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
Device class Class 2
Regulation 21 CFR 888.3560
510(k) K912245
Record published 2015-10-24
Record revised 2025-05-30 (version 5)

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

Catalogue Numbers

Catalogue numbers for AGC Tradition Knee System
Catalogue number Size Status
151075 10 MM 80 MM In distribution
151154 22 MM 71/75 MM In distribution
151118 22 MM 63/67 MM In distribution
151035 10 MM 63/67 MM In distribution
151164 20 MM 87/91 MM In distribution
151047 14 MM 79/83 MM In distribution
151144 24 MM 59 MM In distribution
151150 24 MM 63/67 MM In distribution
151081 12 MM 85 MM In distribution
151049 18 MM 79/83 MM In distribution
151076 12 MM 80 MM In distribution
151033 16 MM 59 MM In distribution
151050 10 MM 87/91 MM In distribution
151072 14 MM 75 MM In distribution
151162 24 MM 79/83 MM In distribution
151052 14 MM 87/91 MM In distribution
151023 16 MM 87/91 MM In distribution
151031 12 MM 59 MM In distribution
151038 16 MM 63/67 MM In distribution
151120 24 MM 63/67 MM In distribution
151087 20 MM 75 MM In distribution
151110 20 MM 59 MM In distribution
151126 24 MM 71/75 MM In distribution
151124 22 MM 71/75 MM In distribution
151014 18 MM 71/75 MM In distribution
151003 16 MM 59 MM In distribution
151008 16 MM 63/67 MM In distribution
151006 12 MM 63/67 MM In distribution
151086 20 MM 70 MM In distribution
151005 10 MM 63/67 MM In distribution
151080 10 MM 85 MM In distribution
151018 16 MM 79/83 MM In distribution
151041 12 MM 71/75 MM In distribution
151158 20 MM 79/83 MM In distribution
151068 16 MM 70 MM In distribution
151064 18 MM 65 MM In distribution
151016 12 MM 79/83 MM In distribution
151062 14 MM 65 MM In distribution
151088 20 MM 80 MM In distribution
151010 10 MM 71/75 MM In distribution
151020 10 MM 87/91 MM In distribution
151073 16 MM 75 MM In distribution
151065 10 MM 70 MM In distribution
151089 20 MM 85 MM In distribution
151002 14 MM 59 MM In distribution
151140 20 MM 59 MM In distribution
151042 14 MM 71/75 MM In distribution
151079 18 MM 80 MM In distribution
151029 8 MM 70 MM In distribution
151036 12 MM 63/67 MM In distribution
151082 14 MM 85 MM In distribution
151040 10 MM 71/75 MM In distribution
151051 12 MM 87/91 MM In distribution
151043 16 MM 71/75 MM In distribution
151116 20 MM 63/67 MM In distribution
151142 22 MM 59 MM In distribution
151069 18 MM 70 MM In distribution
151028 8 MM 65 MM In distribution
151044 18 MM 71/75 MM In distribution
151039 18 MM 63/67 MM In distribution
151012 14 MM 71/75 MM In distribution
151083 16 MM 85 MM In distribution
151085 20 MM 65 MM In distribution
151048 16 MM 79/83 MM In distribution
151146 20 MM 63/67 MM In distribution
151070 10 MM 75 MM In distribution
151074 18 MM 75 MM In distribution
151054 18 MM 87/91 MM In distribution
151011 12 MM 71/75 MM In distribution
151130 22 MM 79/83 MM In distribution
151152 20 MM 71/75 MM In distribution
151066 12 MM 70 MM In distribution
151046 12 MM 79/83 MM In distribution
151037 14 MM 63/67 MM In distribution
151071 12 MM 75 MM In distribution
151084 18 MM 85 MM In distribution
151156 24 MM 71/75 MM In distribution
151007 14 MM 63/67 MM In distribution
151034 18 MM 59 MM In distribution
151061 12 MM 65 MM In distribution
151132 24 MM 79/83 MM In distribution
151063 16 MM 65 MM In distribution
151030 10 MM 59 MM In distribution
151017 14 MM 79/83 MM In distribution
151053 16 MM 87/91 MM In distribution
151024 18 MM 87/91 MM In distribution
151067 14 MM 70 MM In distribution
151160 22 MM 79/83 MM In distribution
151032 14 MM 59 MM In distribution
151045 10 MM 79/83 MM In distribution
151019 18 MM 79/83 MM In distribution
151060 10 MM 65 MM In distribution
151148 22 MM 63/67 MM In distribution
151077 14 MM 80 MM In distribution
151078 16 MM 80 MM In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Prophecy® Microport Orthopedics Inc. 4,423
Exult Knee Replacement System Corentec Co., Ltd. 1,770
Freedom Maxx Orthopedics Inc. 1,693
Legion Smith & Nephew, Inc. 1,534
MyKnee Medacta International SA 1,466
Journey Smith & Nephew, Inc. 1,339
Persona® Zimmer, Inc. 1,254
DJO Surgical Encore Medical, L.P. 1,131
U2 Total Knee System United Orthopedic Corp. 1,078
CKS Plus Shalby Advanced Technologies, Inc. 1,024
Lospa Modular Knee System Corentec Co., Ltd. 1,020
Natural-Knee® Zimmer, Inc. 980

Showing 12 of 1,175. All products under Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K080528 2008-06-17
K022586 2002-08-15

Recalls Naming This Product

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

Recalls naming the identifiers of AGC Tradition Knee System
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Biomet, Inc. 510(k) number 2019-03-01 Class II Packaging process control Two lengths of the 6.5mm RingLoc Hip System Self-Tapping Bone Screw may have the potential for the 30mm screws to be packaged as 20mm screws and vice versa. 809 total 2020-05-27
Biomet, Inc. 510(k) number 2019-03-01 Class II Packaging process control Two lengths of the 6.5mm RingLoc Hip System Self-Tapping Bone Screw may have the potential for the 30mm screws to be packaged as 20mm screws and vice versa. 809 units total 2020-05-27
Biomet, Inc. 510(k) number 2018-12-21 Class II Under Investigation by firm Vanguard Knee System Series-A Standard Patella a potential commingle that could result in the size of the implant not matching the size on the label. 90 units 2020-05-13
Biomet, Inc. 510(k) number 2018-05-24 Class II Under Investigation by firm Two lots of tibial bearings were commingled. There is a possibility that a 14mm tibial bearing is packaged in a box labeled as 12 mm tibial bearing and vice versa. This may lead to extension of surgery to find another implant. 48 2020-04-07
Biomet, Inc. 510(k) number 2018-05-18 Class II Under Investigation by firm One lot of 75mm tibial tray is potentially etched and labeled as a 79 mm tibial tray. This may lead to delay in surgery, or immediate revision surgery to remove an incorrectly sized tibial component after it has been cemented. 16 2020-03-31
Biomet, Inc. 510(k) number 2018-05-11 Class II Under Investigation by firm The label master file was errantly set up as a 63/37mm instead of a 63/67mm. There is no 63/37 size offered, and the product is laser marked with the correct size. 169 2019-11-21
Biomet, Inc. 510(k) number 2017-08-25 Class II Process change control The affected AGC 2000 LP Patella products were over-molded leaving the outside diameter nonconforming to the print dimension. 28 devices 2018-08-09
Biomet, Inc. 510(k) number 2017-08-25 Class II Process change control The affected AGC 2000 LP Patella products were over-molded leaving the outside diameter nonconforming to the print dimension. 11 devices 2018-08-09

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