Catalog Number

-

Brand Name

Single Use Circular Stapler

Version/Model Number

CSA23

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

K162707,K162707

Product Code

GDW

Product Code Name

Staple, Implantable

Public Device Record Key

4d0bccbe-8424-4ba5-8ae3-b5cb6bff9804

Public Version Date

June 21, 2019

Public Version Number

1

DI Record Publish Date

June 13, 2019

Package DI Number

16946912215020

Quantity per Package

6

Contains DI Package

06946912215023

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-