FDA.reportPublic FDA data

BENCOX Hip System

Primary DI
08806373833328
Brand
BENCOX Hip System
Company
Corentec Co., Ltd
Model
01.01.904
Device description
BENCOX II STEM(Blasting)
Published
2015-10-16
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
KWYProsthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented
LPHProsthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
KWYProsthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or UncementedOrthopedic2
LPHProsthesis, Hip, Semi-Constrained, Metal/Polymer, Porous UncementedOrthopedic2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K103431000
K120924000
K122099000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K103431000COREN TOTAL HIP SYSTEMCorentec Co., Ltd.2011-07-21LPH
K120924000BENCOX MIRABO CUP BENCOX MIRABO INSERT (STANDARD& ELEVATED TYES) BENCOX MIRABO CUP SCREW HOLE PLUGCorentec Co., Ltd.2012-09-10LPH
K122099000BENCOX II STEM, BENCOX METAL HEADCorentec Co., Ltd.2012-10-05LPH

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
08806373833328PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
08806373833328088063738333288806373833328

GMDN Terms#

Term, Definition table
TermDefinition
Press-fit femoral stem prosthesisA sterile implantable device designed to replace the proximal femoral neck as part of a total hip arthroplasty (THA). The device is contoured to enable fixation by pressing the distal end into the cortex of the remaining natural femur to achieve a mechanical interlock without the use of bone cement. The device is made of metal [e.g., cobalt-chrome (Co-Cr), titanium (Ti), stainless steel].

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

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