MADISON - IMPLANET

Duns Number:291993439

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More Product Details

Catalog Number

540343

Brand Name

MADISON

Version/Model Number

UC insert trial size 4 - 18mm

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

Product Characteristics

MRI safety Status

Labeling does not contain MRI Safety Information

Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)

-

Device labeled as "Not made with natural rubber latex"

-

For Single-Use

-

Prescription Use (Rx)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

K192084

Product Code Details

Product Code

JWH

Product Code Name

Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer

Device Record Status

Public Device Record Key

93c6f812-1296-404f-a738-12532b587a82

Public Version Date

March 24, 2020

Public Version Number

1

DI Record Publish Date

March 16, 2020

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"IMPLANET" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 236
2 A medical device with a moderate to high risk that requires special controls. 828