Catalog Number

-

Brand Name

Empower

Version/Model Number

1A1-1=R30-6/1-4

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)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

ISW

Product Code Name

Assembly, Knee/Shank/Ankle/Foot, External

Public Device Record Key

adcb74d3-4dc0-4c36-89d0-d63d3676c71e

Public Version Date

May 14, 2018

Public Version Number

1

DI Record Publish Date

April 11, 2018

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-