Catalog Number

-

Brand Name

VIVE

Version/Model Number

SUP2039

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

eedec9c4-cc6a-4e05-8fdd-6b2af0919c5e

Public Version Date

January 20, 2020

Public Version Number

1

DI Record Publish Date

January 12, 2020

Package DI Number

10810041981148

Quantity per Package

1

Contains DI Package

00810041981141

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case