ANATOMIC

Primary DI
03701089500760
Brand
ANATOMIC
Company
AMPLITUDE SAS
Model
1-0209904
Catalog number
1-0209904
Device description
ANATOMIC® Tibial Base Plate for Fixed Bearing Insert Cemented Size 4
Published
2017-08-08
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
K161414000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K161414000Anatomic Total Knee SystemAmplitude2017-01-19JWH

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
03701089500760PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
03701089500760037010895007603701089500760

GMDN Terms#

Term, Definition table
TermDefinition
Uncoated knee tibia prosthesis, metallicAn implantable device designed to replace the tibial condyles (tibial 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 an insert and/or the femoral prosthetic component of the knee joint and its implantation is intended to be performed with bone cement.

Sterilization Methods#

Method table
Method

Contacts#

Phone, Email table
PhoneEmail
+0033475418741regulatoryaffairs@amplitude-ortho.com

Regulatory Flags#

DUNS number
634855407
Device count
1
Lot or batch
true
Expiration date on label
true
No natural rubber latex
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
03701089501071VENTO Fixation Screw1-01-12-91452017-12-22
03701089514309VENTO Fixation Screw1-01-12-91152017-12-11
03701089514316VENTO Fixation Screw1-01-12-91202017-12-18
03701089514323VENTO Fixation Screw1-01-12-91252017-12-18
03701089514330VENTO Fixation Screw1-01-12-91302017-12-18
03701089514347VENTO Fixation Screw1-01-12-91352017-12-18
03701089514354VENTO Fixation Screw1-01-12-91402017-12-18
03701089514361VENTO Fixation Screw1-01-12-91502017-12-18
03701089514378VENTO Fixation Screw1-01-12-91552017-12-18
03701089514385VENTO Fixation Screw1-01-12-91602017-12-18
03701089514392VENTO Fixation Screw1-01-12-91652017-12-18
03701089514408VENTO Fixation Screw1-01-12-91702017-12-18
03701089500814AMPLITUDE1-02100301-02100302017-08-07
03701089500821AMPLITUDE1-02100331-02100332017-08-08
03701089500838AMPLITUDE1-02100361-02100362017-08-08
03701089500845AMPLITUDE1-02100391-02100392017-08-08
03701089524124Crescendo Patella Component 28x6mm 1-01-07-70012018-10-16
03701089524131Crescendo Patella Component 30x7mm1-01-07-70022018-10-16
03701089524148Crescendo Patella Component 32x8mm 1-01-07-70032018-10-16
03701089524155Crescendo Patella Component 35x9mm1-01-07-70042018-10-16

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Primary DI, Brand, Company table
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