FDA.reportPublic FDA data

LOSPA Total Knee System

Primary DI
08806373821189
Brand
LOSPA Total Knee System
Company
Corentec Co., Ltd
Model
01.10.148
Device description
LOSPA Tibial Insert (CR)
Published
2015-10-08
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
Sterile
true
Single use
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
K110404000
K130673000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K110404000EAUM TOTAL KNEE SYSTEMCorentec Co., Ltd.2012-02-16JWH
K130673000LOSPA TOTAL KNEE REPLACEMENT SYSTEMCorentec Co., Ltd.2013-04-15JWH

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
08806373821189PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
08806373821189088063738211898806373821189

GMDN Terms#

Term, Definition table
TermDefinition
Uncoated knee tibia/insert prosthesisA sterile implantable device designed to replace the tibial condyles (tibial component) during primary bicondylar replacement of the knee joint or to replace a dysfunctional knee prosthesis (revision). It is made of metal [e.g., cobalt-chrome (Co-Cr)] and is not coated with a material intended to improve fixation and stability by promoting bone ingrowth; it includes a polyethylene (PE) insert/platform for femoral articulation. Device implantation is intended to be performed with bone cement.

Contacts#

Phone, Email table
PhoneEmail
+820415857114hckoh@corentec.com

Regulatory Flags#

DUNS number
688739895
Device count
1
Lot or batch
true
Expiration date on label
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
08800017261850EXULT Knee Replacement SystemK3.IAX.3657-09T2020-01-09
08800017261867EXULT Knee Replacement SystemK3.IAX.3657-10T2020-01-09
08800017261874EXULT Knee Replacement SystemK3.IAX.3657-11T2020-01-09
08800017261881EXULT Knee Replacement SystemK3.IAX.3657-12T2020-01-09
08800017261898EXULT Knee Replacement SystemK3.IAX.3657-13T2020-01-09
08800017261904EXULT Knee Replacement SystemK3.IAX.3657-14T2020-01-09
08800017261911EXULT Knee Replacement SystemK3.IAX.3657-16T2020-01-09
08800017261928EXULT Knee Replacement SystemK3.IAX.3657-18T2020-01-09
08800017267494EXULT Knee Replacement SystemK3.IAX.3657-20T2020-01-09
08800017267500EXULT Knee Replacement SystemK3.IAX.3657-22T2020-01-09
08800017267517EXULT Knee Replacement SystemK3.IAX.3657-24T2020-01-09
08800017262925EXULT Knee Replacement SystemK3.IBN.4266-12T2020-01-10
08800017262932EXULT Knee Replacement SystemK3.IBN.4266-13T2020-01-10
08800017262949EXULT Knee Replacement SystemK3.IBN.4266-14T2020-01-10
08800017262956EXULT Knee Replacement SystemK3.IBN.4266-16T2020-01-10
08800017262963EXULT Knee Replacement SystemK3.IBN.4266-18T2020-01-10
08800017262970EXULT Knee Replacement SystemK3.IBN.4469-09T2020-01-10
08800017262987EXULT Knee Replacement SystemK3.IBN.4469-10T2020-01-10
08800017262994EXULT Knee Replacement SystemK3.IBN.4469-11T2020-01-10
08800017263007EXULT Knee Replacement SystemK3.IBN.4469-12T2020-01-10

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
00885556923023NASmith & Nephew, Inc.JWH2026-07-16
08800017262819EXULT Knee Replacement SystemCorentec Co., LtdJWH2020-01-10
08800017262826EXULT Knee Replacement SystemCorentec Co., LtdJWH2020-01-10
08800017262833EXULT Knee Replacement SystemCorentec Co., LtdJWH2020-01-10
08800017262840EXULT Knee Replacement SystemCorentec Co., LtdJWH2020-01-10
08800017262857EXULT Knee Replacement SystemCorentec Co., LtdJWH2020-01-10
08800017262864EXULT Knee Replacement SystemCorentec Co., LtdJWH2020-01-10
08800017262871EXULT Knee Replacement SystemCorentec Co., LtdJWH2020-01-10
08800017262888EXULT Knee Replacement SystemCorentec Co., LtdJWH2020-01-10
08800017262895EXULT Knee Replacement SystemCorentec Co., LtdJWH2020-01-10
08800017262901EXULT Knee Replacement SystemCorentec Co., LtdJWH2020-01-10
08800017262918EXULT Knee Replacement SystemCorentec Co., LtdJWH2020-01-10
08800017262925EXULT Knee Replacement SystemCorentec Co., LtdJWH2020-01-10
08800017262932EXULT Knee Replacement SystemCorentec Co., LtdJWH2020-01-10
08800017262949EXULT Knee Replacement SystemCorentec Co., LtdJWH2020-01-10
08800017262956EXULT Knee Replacement SystemCorentec Co., LtdJWH2020-01-10
08800017262963EXULT Knee Replacement SystemCorentec Co., LtdJWH2020-01-10
08800017262970EXULT Knee Replacement SystemCorentec Co., LtdJWH2020-01-10
08800017262987EXULT Knee Replacement SystemCorentec Co., LtdJWH2020-01-10
08800017262994EXULT Knee Replacement SystemCorentec Co., LtdJWH2020-01-10
08800017263007EXULT Knee Replacement SystemCorentec Co., LtdJWH2020-01-10
08800017263014EXULT Knee Replacement SystemCorentec Co., LtdJWH2020-01-10
08800017263021EXULT Knee Replacement SystemCorentec Co., LtdJWH2020-01-10
08800017263038EXULT Knee Replacement SystemCorentec Co., LtdJWH2020-01-10
08800017263045EXULT Knee Replacement SystemCorentec Co., LtdJWH2020-01-10
08800017263052EXULT Knee Replacement SystemCorentec Co., LtdJWH2020-01-10
08800017263069EXULT Knee Replacement SystemCorentec Co., LtdJWH2020-01-10
08800017263076EXULT Knee Replacement SystemCorentec Co., LtdJWH2020-01-10
08800017263083EXULT Knee Replacement SystemCorentec Co., LtdJWH2020-01-10
08800017263090EXULT Knee Replacement SystemCorentec Co., LtdJWH2020-01-10