Catalog Number

-

Brand Name

Vive

Version/Model Number

SUP2004BLKS

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

bc3f39f0-22a8-477d-bed7-25c0eec38a6f

Public Version Date

August 08, 2022

Public Version Number

1

DI Record Publish Date

July 31, 2022

Package DI Number

10850041211876

Quantity per Package

40

Contains DI Package

00850041211879

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case