FDA.reportPublic FDA data

NovoKnee Total Knee System

Primary DI
00811382039096
Brand
NovoKnee Total Knee System
Company
Novosource, LLC
Model
3115-1201
Catalog number
3115-1201
Device description
Size 1 CR Right Femoral Trial Stainless Steel
Published
2023-08-18
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
JWHProsthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
JWHProsthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/PolymerOrthopedic2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K131398000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K131398000NOVOKNEE TOTAL KNEE SYSTEMNovosource, Inc.2013-09-16JWH

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00811382039096PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00811382039096008113820390968113820390960811382039096

GMDN Terms#

Term, Definition table
TermDefinition
Knee femur prosthesis trial, reusableA copy of a final femur prosthesis designed to be used during unicompartmental knee replacement surgery or total knee arthroplasty (TKA) to determine the correct alignment, size, and fit of the final prosthesis. It is one of a set, or a set, of graduated sizes, and may be used in conjunction with a knee tibia trial prosthesis and a patella trial prosthesis. It is typically made of metal or polymer material and includes femoral articulation trials, femoral spacer trials, femoral wedge/augment trials, anterior stop trials, stem adaptor trials, and stem trials. This is a reusable device.

Device Sizes#

Type, Value, Unit table
TypeValueUnit
Device Size Text, specify0

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Contacts#

Phone, Email table
PhoneEmail
3045542167info@novosource.com

Regulatory Flags#

DUNS number
081034828
Device count
1
Lot or batch
true
Sterilization required before use
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00811382037658NovoHip Total Hip System1500-10161500-10162020-05-26
00811382037672NovoKnee Total Knee System3220-50243220-50242020-05-26
00811382037689NovoHip Total Hip System1345-36011345-36012020-11-03
00811382037696NovoHip Total Hip System1345-36021345-36022020-11-03
00811382037702NovoHip Total Hip System1345-36031345-36032020-11-03
00811382037719NovoHip Total Hip System1345-36041345-36042020-11-03
00811382037795NovoHip Total Hip System1345-28011345-28012021-04-20
00811382037801NovoHip Total Hip System1345-28021345-28022021-04-20
00811382037818NovoHip Total Hip System1345-28031345-28032021-04-20
00811382037825NovoHip Total Hip System1345-32011345-32012021-04-20
00811382037832NovoHip Total Hip System1345-32021345-32022021-04-20
00811382037849NovoHip Total Hip System1345-32031345-32032021-04-20
00811382037856NovoHip Total Hip System1345-32041345-32042021-04-20
00811382037726NovoKnee Total Knee System3120-51003120-51002024-07-19
00811382039287NovoHip Total Hip System1445-28051445-28052024-04-09
00811382039294NovoHip Total Hip System1445-32051445-32052024-04-09
00811382039300NovoHip Total Hip System1445-36051445-36052024-04-09
00811382039089NovoKnee Total Knee System3115-11013115-11012023-08-18
00811382039102NovoKnee Total Knee System3115-11023115-11022023-08-18
00811382039119NovoKnee Total Knee System3115-12023115-12022023-08-18

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
00840097536705Identity CR KARestor3d, Inc.JWH2026-09-25
00840097536712Identity CR KARestor3d, Inc.JWH2026-09-25
00840097536729Identity CR KA 3DP PorousRestor3d, Inc.JWH2026-09-25
00840097536736Identity CR KA 3DP PorousRestor3d, Inc.JWH2026-09-25
00840097536743Identity CR KA 3DP PorousRestor3d, Inc.JWH2026-09-25
00840097536750Identity CR KA 3DP PorousRestor3d, Inc.JWH2026-09-25
00840097536767Identity CR KA 3DP PorousRestor3d, Inc.JWH2026-09-25
00840097536774Identity CR KA 3DP PorousRestor3d, Inc.JWH2026-09-25
00840097536781Identity CR KARestor3d, Inc.JWH2026-09-25
00840097536798Identity CR KARestor3d, Inc.JWH2026-09-25
00840097536804Identity CR KA 3DP PorousRestor3d, Inc.JWH2026-09-25
00840097536811Identity CR KA 3DP PorousRestor3d, Inc.JWH2026-09-25
E31442411410SignatureMaterialise NVJWH2026-09-24
E31442422415SignatureMaterialise NVJWH2026-09-24
E31442422450SignatureMaterialise NVJWH2026-09-24
E31442422451SignatureMaterialise NVJWH2026-09-24
E31442422452SignatureMaterialise NVJWH2026-09-24
E31442422453SignatureMaterialise NVJWH2026-09-24
E31442422455SignatureMaterialise NVJWH2026-09-24
E31442422456SignatureMaterialise NVJWH2026-09-24
E31442422457SignatureMaterialise NVJWH2026-09-24
E31442422458SignatureMaterialise NVJWH2026-09-24
E31442422460SignatureMaterialise NVJWH2026-09-24
E31442422461SignatureMaterialise NVJWH2026-09-24
E31442422462SignatureMaterialise NVJWH2026-09-24
E31442422463SignatureMaterialise NVJWH2026-09-24
E31442422465SignatureMaterialise NVJWH2026-09-24
E31442422466SignatureMaterialise NVJWH2026-09-24
E31442422467SignatureMaterialise NVJWH2026-09-24
E31442422468SignatureMaterialise NVJWH2026-09-24