Catalog Number

-

Brand Name

ABTHERA™

Version/Model Number

370605

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

MR Conditional

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

K090489,K090489

Product Code

FTL

Product Code Name

Mesh, Surgical, Polymeric

Public Device Record Key

915c7823-3832-49c4-8621-5d7fd263d036

Public Version Date

September 09, 2020

Public Version Number

5

DI Record Publish Date

September 05, 2016

Package DI Number

00849554000223

Quantity per Package

5

Contains DI Package

00849554001268

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

5 PACK