Catalog Number

5444-5-110

Brand Name

MEDPOR

Version/Model Number

5444-5-110

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

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

Yes

Prescription Use (Rx)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

FWP

Product Code Name

PROSTHESIS, CHIN, INTERNAL

Public Device Record Key

f11bec40-17f9-4c11-b243-1cd53e753ae5

Public Version Date

September 17, 2019

Public Version Number

1

DI Record Publish Date

September 09, 2019

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-