Catalog Number

-

Brand Name

SimuPlus™

Version/Model Number

7700FB42

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

MR Safe

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

Yes

Prescription Use (Rx)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K201449

Product Code

KRH

Product Code Name

RING, ANNULOPLASTY

Public Device Record Key

0cd09f62-db36-42fe-b42e-614148117555

Public Version Date

May 24, 2021

Public Version Number

1

DI Record Publish Date

May 15, 2021

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-