Catalog Number

-

Brand Name

VIVE

Version/Model Number

SUP1030

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

ITQ

Product Code Name

Joint, Knee, External Brace

Public Device Record Key

428150b8-59f7-411c-aa50-f3fdc4139721

Public Version Date

September 05, 2022

Public Version Number

2

DI Record Publish Date

January 16, 2019

Package DI Number

10818323025764

Quantity per Package

40

Contains DI Package

00818323025767

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case