Catalog Number

-

Brand Name

ILA

Version/Model Number

3975

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

October 01, 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

-

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

K885222

Product Code

GDW

Product Code Name

STAPLE, IMPLANTABLE

Public Device Record Key

967797b8-be06-446d-8292-25b8effb9fb4

Public Version Date

April 12, 2022

Public Version Number

4

DI Record Publish Date

August 28, 2015

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-