Catalog Number

C-HYB-20X30

Brand Name

Zenapro

Version/Model Number

G23770

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

May 14, 2018

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

K111695

Product Code

FTL

Product Code Name

Mesh, surgical, polymeric

Public Device Record Key

16c6a18b-ed9b-488e-890b-058ae604b542

Public Version Date

June 10, 2022

Public Version Number

7

DI Record Publish Date

November 03, 2015

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-