Medial Rotation Knee

Primary DI
05055455503489
Brand
Medial Rotation Knee
Company
MATORTHO LTD
Model
156-025
Catalog number
156-025
Device description
Medial Rotation Knee Femoral Component Pegged Right F5
Published
2015-05-12
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

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
K020214000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K020214000MEDIAL ROTATION KNEE SYSTEMEngineering Consulting Services, Inc.2002-02-26JWH

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
05055455503489PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
05055455503489050554555034895055455503489

GMDN Terms#

Term, Definition table
TermDefinition
Uncoated knee femur prosthesis, metallicAn implantable device designed to replace the femoral condyles (femoral component) during primary bicondylar replacement of the knee joint, femoral bone resection, or to replace a dysfunctional knee prosthesis (revision); it is made of metal [e.g., cobalt-chrome (Co-Cr), cobalt-chrome-molybdenum (Co-Cr-Mo), titanium (Ti)] and is not coated with a material intended to improve fixation and stability by promoting bone ingrowth. The device is designed to articulate with tibial and, if required, patellar prosthetic components of the knee joint and its implantation is intended to be performed with bone cement.

Sterilization Methods#

Method table
Method

Regulatory Flags#

DUNS number
216819863
Device count
1
Lot or batch
true
Expiration date on label
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
05055455518285SAIPH®293-202293-2002021-01-14
05055455517714SAIPH®290-030290-0302021-01-18
05055455517721SAIPH®290-050290-0502021-01-18
05055455517738SAIPH®290-051290-0512021-01-18
05055455517745SAIPH®290-052290-0522021-01-18
05055455517752SAIPH®290-053290-0532021-01-18
05055455517769SAIPH®290-160290-1602021-01-18
05055455517776SAIPH®290-161290-1612021-01-18
05055455517783SAIPH®290-162290-1622021-01-18
05055455517837SAIPH®290-181290-1812021-01-18
05055455517899SAIPH®290-187290-1872021-01-18
05055455518049SAIPH®293-004293-0042021-01-18
05055455518056SAIPH®293-005293-0052021-01-18
05055455518063SAIPH®293-006293-0062021-01-18
05055455518070SAIPH®293-007293-0072021-01-18
05055455518087SAIPH®293-025293-0252021-01-18
05055455518094SAIPH®293-026293-0262021-01-18
05055455518124SAIPH®293-029293-0292021-01-18
05055455518131SAIPH®293-030293-0302021-01-18
05055455518148SAIPH®293-031293-0312021-01-18

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