Catalog Number

TAB-25

Brand Name

SJM Tailor™

Version/Model Number

Annuloplasty Band

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

K022363

Product Code

KRH

Product Code Name

RING, ANNULOPLASTY

Public Device Record Key

3736af54-1e72-4ec5-a7ef-6a09f3d1cfac

Public Version Date

February 05, 2021

Public Version Number

4

DI Record Publish Date

January 07, 2015

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-