Arthrex®

Primary DI
00888867108004
Brand
Arthrex®
Company
ARTHREX, INC.
Model
AR-513-RC16
Catalog number
AR-513-RC16
Device description
IBAL TKA,BEARING IMP,CR,SZ 2,16MM
Published
2017-02-15
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
MR Conditional
Rx
true
Sterile
true
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
HSXPROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER
JWHPROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
KRRPROSTHESIS, KNEE, PATELLO/FEMORAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER
MBHPROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
HSXProsthesis, Knee, Femorotibial, Non-Constrained, Cemented, Metal/PolymerOrthopedic2
JWHProsthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/PolymerOrthopedic2
KRRProsthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/PolymerOrthopedic2
MBHProsthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/PolymerOrthopedic2

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00888867108004PrimaryGS10
M150AR513RC161SecondaryHIBCC0

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00888867108004008888671080048888671080040888867108004

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.

Sterilization Methods#

Method table
Method

Contacts#

Phone, Email table
PhoneEmail
+1(800)934-4404complaints@arthrex.com

Regulatory Flags#

DUNS number
131747628
Device count
1
Lot or batch
true
Expiration date on label
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00888867084384Arthrex®ABS-3005ABS-30052017-02-15
00888867084407Arthrex®ABS-3008ABS-30082017-02-15
00888867084421Arthrex®ABS-3016ABS-30162017-02-15
00888867084148Arthrex®ABS-2001-01ABS-2001-012017-02-15
00888867084155Arthrex®ABS-2001-02ABS-2001-022017-02-15
00888867084162Arthrex®ABS-2001-05ABS-2001-052017-02-15
00888867084179Arthrex®ABS-2001-10ABS-2001-102017-02-15
00888867084186Arthrex®ABS-2002-01ABS-2002-012017-02-15
00888867084193Arthrex®ABS-2002-05ABS-2002-052017-02-15
00888867084209Arthrex®ABS-2002-10ABS-2002-102017-02-15
00888867084216Arthrex®ABS-2003-05ABS-2003-052017-02-15
00888867084223Arthrex®ABS-2003-10ABS-2003-102017-02-15
00888867084230Arthrex®ABS-2004-01ABS-2004-012017-02-15
00888867084247Arthrex®ABS-2004-03ABS-2004-032017-02-15
00888867084254Arthrex®ABS-2004-08ABS-2004-082017-02-15
00888867614543Arthrex®AR-S8740-16HA-SAR-S8740-16HA-S2026-10-07
00888867614550Arthrex®AR-S8740-18HA-SAR-S8740-18HA-S2026-10-07
00888867614567Arthrex®AR-S8740-20HA-SAR-S8740-20HA-S2026-10-07
00888867614574Arthrex®AR-S8740-22HA-SAR-S8740-22HA-S2026-10-07
00888867614581Arthrex®AR-S8740-24HA-SAR-S8740-24HA-S2026-10-07

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Primary DI, Brand, Company table
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08906067247537Opulent TiNbN Coated KneeMERIL HEALTHCARE PRIVATE LIMITEDJWH2026-10-05