FDA.reportPublic FDA data

LOSPA Total Knee System

Primary DI
08806373821301
Brand
LOSPA Total Knee System
Company
Corentec Co., Ltd
Model
01.10.15C
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
08806373821301PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
08806373821301088063738213018806373821301

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
08800017262178EXULT Knee Replacement SystemK3.IAX.4469-09T2020-01-10
08800017262185EXULT Knee Replacement SystemK3.IAX.4469-10T2020-01-10
08800017262192EXULT Knee Replacement SystemK3.IAX.4469-11T2020-01-10
08800017262208EXULT Knee Replacement SystemK3.IAX.4469-12T2020-01-10
08800017262215EXULT Knee Replacement SystemK3.IAX.4469-13T2020-01-10
08800017262222EXULT Knee Replacement SystemK3.IAX.4469-14T2020-01-10
08800017262239EXULT Knee Replacement SystemK3.IAX.4469-16T2020-01-10
08800017262246EXULT Knee Replacement SystemK3.IAX.4469-18T2020-01-10
08800017262253EXULT Knee Replacement SystemK3.IAX.4572-09T2020-01-10
08800017262260EXULT Knee Replacement SystemK3.IAX.4572-10T2020-01-10
08800017262277EXULT Knee Replacement SystemK3.IAX.4572-11T2020-01-10
08800017262284EXULT Knee Replacement SystemK3.IAX.4572-12T2020-01-10
08800017262291EXULT Knee Replacement SystemK3.IAX.4572-13T2020-01-10
08800017262307EXULT Knee Replacement SystemK3.IAX.4572-14T2020-01-10
08800017262314EXULT Knee Replacement SystemK3.IAX.4572-16T2020-01-10
08800017262321EXULT Knee Replacement SystemK3.IAX.4572-18T2020-01-10
08800017262338EXULT Knee Replacement SystemK3.IAX.4775-09T2020-01-10
08800017262345EXULT Knee Replacement SystemK3.IAX.4775-10T2020-01-10
08800017262352EXULT Knee Replacement SystemK3.IAX.4775-11T2020-01-10
08800017262369EXULT Knee Replacement SystemK3.IAX.4775-12T2020-01-10

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
00885556923023NASmith & Nephew, Inc.JWH2026-07-16
08800017262178EXULT Knee Replacement SystemCorentec Co., LtdJWH2020-01-10
08800017262185EXULT Knee Replacement SystemCorentec Co., LtdJWH2020-01-10
08800017262192EXULT Knee Replacement SystemCorentec Co., LtdJWH2020-01-10
08800017262208EXULT Knee Replacement SystemCorentec Co., LtdJWH2020-01-10
08800017262215EXULT Knee Replacement SystemCorentec Co., LtdJWH2020-01-10
08800017262222EXULT Knee Replacement SystemCorentec Co., LtdJWH2020-01-10
08800017262239EXULT Knee Replacement SystemCorentec Co., LtdJWH2020-01-10
08800017262246EXULT Knee Replacement SystemCorentec Co., LtdJWH2020-01-10
08800017262253EXULT Knee Replacement SystemCorentec Co., LtdJWH2020-01-10
08800017262260EXULT Knee Replacement SystemCorentec Co., LtdJWH2020-01-10
08800017262277EXULT Knee Replacement SystemCorentec Co., LtdJWH2020-01-10
08800017262284EXULT Knee Replacement SystemCorentec Co., LtdJWH2020-01-10
08800017262291EXULT Knee Replacement SystemCorentec Co., LtdJWH2020-01-10
08800017262307EXULT Knee Replacement SystemCorentec Co., LtdJWH2020-01-10
08800017262314EXULT Knee Replacement SystemCorentec Co., LtdJWH2020-01-10
08800017262321EXULT Knee Replacement SystemCorentec Co., LtdJWH2020-01-10
08800017262338EXULT Knee Replacement SystemCorentec Co., LtdJWH2020-01-10
08800017262345EXULT Knee Replacement SystemCorentec Co., LtdJWH2020-01-10
08800017262352EXULT Knee Replacement SystemCorentec Co., LtdJWH2020-01-10
08800017262369EXULT Knee Replacement SystemCorentec Co., LtdJWH2020-01-10
08800017262376EXULT Knee Replacement SystemCorentec Co., LtdJWH2020-01-10
08800017262383EXULT Knee Replacement SystemCorentec Co., LtdJWH2020-01-10
08800017262390EXULT Knee Replacement SystemCorentec Co., LtdJWH2020-01-10
08800017262406EXULT Knee Replacement SystemCorentec Co., LtdJWH2020-01-10
08800017262413EXULT Knee Replacement SystemCorentec Co., LtdJWH2020-01-10
08800017262420EXULT Knee Replacement SystemCorentec Co., LtdJWH2020-01-10
08800017262437EXULT Knee Replacement SystemCorentec Co., LtdJWH2020-01-10
08800017262444EXULT Knee Replacement SystemCorentec Co., LtdJWH2020-01-10
08800017262451EXULT Knee Replacement SystemCorentec Co., LtdJWH2020-01-10