FDA.reportPublic FDA data

Genflex2 Total Knee System

Primary DI
10840843112600
Brand
Genflex2 Total Knee System
Company
Stelkast Incorporated
Model
SC3751-6
Device description
Genflex2 CR Femur, Size 6, Left
Published
2016-09-20
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
OTC
false
Sterile
true
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
OIYProsthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer + Additive/Metal/Polymer + Additive

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
OIYProsthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer + Additive/Metal/Polymer + AdditiveOrthopedic2

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
10840843112600PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized table
Source identifierGTIN-14 normalized
1084084311260010840843112600

GMDN Terms#

Term, Definition table
TermDefinition
Uncoated knee femur prosthesis, metallicAn implantable device designed to replace the femoral condyles (femoral component) during primary bicondylar replacement of the knee joint, femoral bone resection, or to replace a dysfunctional knee prosthesis (revision); it is made of metal [e.g., cobalt-chrome (Co-Cr), cobalt-chrome-molybdenum (Co-Cr-Mo), titanium (Ti)] and is not coated with a material intended to improve fixation and stability by promoting bone ingrowth. The device is designed to articulate with tibial and, if required, patellar prosthetic components of the knee joint and its implantation is intended to be performed with bone cement.

Sterilization Methods#

Method table
Method

Contacts#

Phone, Email table
PhoneEmail
1(724)941-6368customer_service@stelkast.com

Regulatory Flags#

DUNS number
804792265
Device count
1
DM exempt
false
Premarket exempt
true
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
false
Expiration date on label
true
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
false

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
10840843100157Provident Hip SystemSC1217-462015-03-03
10840843100164Provident Hip SystemSC1217-482015-04-15
10840843100171Provident Hip SystemSC1217-502015-04-15
10840843100188Provident Hip SystemSC1217-522015-04-15
10840843100195Provident Hip SystemSC1217-542015-04-15
10840843100201Provident Hip SystemSC1217-562015-04-15
10840843100218Provident Hip SystemSC1217-582015-04-15
10840843100225Provident Hip SystemSC1217-602015-04-15
10840843100232Provident Hip SystemSC1217-622015-04-15
10840843100249Provident Hip SystemSC1217-642015-04-15
10840843100256Provident Hip SystemSC1217-662015-04-15
10840843100263Provident Hip SystemSC1217-682015-04-15
10840843100270Provident Hip SystemSC1217-702015-04-15
10840843100287Provident Hip SystemSC1217-722015-04-15
10840843100805Zirconia Ceramic HeadSC1405-28mm +0M2015-10-07
10840843100812Zirconia Ceramic HeadSC1405-28mm +3.5 L2015-10-07
10840843100829Zirconia Ceramic HeadSC1405-28mm -3.5 S2015-10-07
10840843100836Zirconia Ceramic HeadSC1406-28mm +7 XL2015-10-07
10840843100843Proform Hip SystemSC1408-100-462015-02-17
10840843100850Proform Hip SystemSC1408-100-482015-02-17

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
00889024704695Vanguard XP® Complete Knee SystemBiomet Orthopedics, LLCOIY2026-01-27
00889024704619Vanguard XP® Complete Knee SystemBiomet Orthopedics, LLCOIY2026-01-08
00889024704749Vanguard XP® Complete Knee SystemBiomet Orthopedics, LLCOIY2026-01-08
00889024704862Vanguard XP® Complete Knee SystemBiomet Orthopedics, LLCOIY2026-01-08
00889024704541Vanguard XP® Complete Knee SystemBiomet Orthopedics, LLCOIY2025-12-23
00889024704565Vanguard XP® Complete Knee SystemBiomet Orthopedics, LLCOIY2025-12-23
00889024704589Vanguard XP® Complete Knee SystemBiomet Orthopedics, LLCOIY2025-12-23
00889024704657Vanguard XP® Complete Knee SystemBiomet Orthopedics, LLCOIY2025-12-23
00889024704664Vanguard XP® Complete Knee SystemBiomet Orthopedics, LLCOIY2025-12-23
00889024704718Vanguard XP® Complete Knee SystemBiomet Orthopedics, LLCOIY2025-12-23
00889024704763Vanguard XP® Complete Knee SystemBiomet Orthopedics, LLCOIY2025-12-23
00889024704824Vanguard XP® Complete Knee SystemBiomet Orthopedics, LLCOIY2025-12-23
00889024704848Vanguard XP® Complete Knee SystemBiomet Orthopedics, LLCOIY2025-12-23
00889024658134Persona® Knee SystemZimmer, Inc.OIY2025-02-06
00889024658165Persona® Knee SystemZimmer, Inc.OIY2025-02-06
00889024658189Persona® Knee SystemZimmer, Inc.OIY2025-02-06
00889024658226Persona® Knee SystemZimmer, Inc.OIY2025-02-06
00889024658264Persona® Knee SystemZimmer, Inc.OIY2025-02-06
00889024658295Persona® Knee SystemZimmer, Inc.OIY2025-02-06
00889024658301Persona® Knee SystemZimmer, Inc.OIY2025-02-06
00889024658363Persona® Knee SystemZimmer, Inc.OIY2025-02-06
00889024658400Persona® Knee SystemZimmer, Inc.OIY2025-02-06
00889024658417Persona® Knee SystemZimmer, Inc.OIY2025-02-06
00889024658455Persona® Knee SystemZimmer, Inc.OIY2025-02-06
00889024658493Persona® Knee SystemZimmer, Inc.OIY2025-02-06
00889024658516Persona® Knee SystemZimmer, Inc.OIY2025-02-06
00889024658523Persona® Knee SystemZimmer, Inc.OIY2025-02-06
00889024658561Persona® Knee SystemZimmer, Inc.OIY2025-02-06
00889024658622Persona® Knee SystemZimmer, Inc.OIY2025-02-06
00889024658653Persona® Knee SystemZimmer, Inc.OIY2025-02-06