Catalog Number

4041

Brand Name

SU-POR Surgical Implant

Version/Model Number

4041

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

April 09, 2019

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

K140437

Product Code

FWP

Product Code Name

Prosthesis, Chin, Internal

Public Device Record Key

940a4a4a-46da-4245-89de-597cb539e295

Public Version Date

September 15, 2021

Public Version Number

4

DI Record Publish Date

March 01, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-