Catalog Number

4002

Brand Name

SU-POR Surgical Implant

Version/Model Number

4002

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

MR Safe

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

24c96840-5036-4f32-96c8-416292a85be0

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

January 15, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-