Catalog Number

FTRG-1X10

Brand Name

Fortify

Version/Model Number

G59059

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

K191696,K980431

Product Code

FTM

Product Code Name

Mesh, surgical

Public Device Record Key

4249e5e7-7e3f-4fb4-aa78-2d4a5532e8ca

Public Version Date

June 10, 2022

Public Version Number

3

DI Record Publish Date

May 07, 2021

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-