Catalog Number

-

Brand Name

ProGrip

Version/Model Number

PP1208DR

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K140941

Product Code

FTL

Product Code Name

Mesh, surgical, polymeric

Public Device Record Key

f9e5a0d7-7105-47d7-a63b-fd7dc25bb1e0

Public Version Date

September 14, 2022

Public Version Number

4

DI Record Publish Date

September 04, 2021

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-