Catalog Number

-

Brand Name

Walgreens

Version/Model Number

920165

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

-

Prescription Use (Rx)

-

Over the Counter (OTC)

Yes

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

ITW

Product Code Name

Joint, Ankle, External Brace

Public Device Record Key

1e998733-92ef-418f-b5f9-4cde744406f8

Public Version Date

May 26, 2020

Public Version Number

1

DI Record Publish Date

May 18, 2020

Package DI Number

10049022867038

Quantity per Package

12

Contains DI Package

00049022867031

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Carton