Catalog Number

MFP301

Brand Name

TiO2Mesh

Version/Model Number

MFP301

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In HIBCC

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"

Yes

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

K113311

Product Code

FTL

Product Code Name

Mesh, Surgical, Polymeric

Public Device Record Key

69cc06f0-1bb7-4c7e-ba4b-e0d49086f41a

Public Version Date

June 10, 2022

Public Version Number

5

DI Record Publish Date

March 15, 2018

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-