Catalog Number

-

Brand Name

SurgiMesh

Version/Model Number

T1115-8

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)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K061445,K061445

Product Code

FTL

Product Code Name

Mesh, Surgical, Polymeric

Public Device Record Key

87650f0c-1c35-4ebd-82db-02237c271bf7

Public Version Date

June 10, 2022

Public Version Number

4

DI Record Publish Date

January 30, 2020

Package DI Number

10850011929220

Quantity per Package

5

Contains DI Package

00850011929223

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case