Catalog Number

9106-1111

Brand Name

UTF™ Stem

Version/Model Number

9106-1111

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

HWR

Product Code Name

Driver, Prosthesis

Public Device Record Key

9ea09e71-8e68-4987-9006-fb6a170df7a6

Public Version Date

April 23, 2019

Public Version Number

7

DI Record Publish Date

June 26, 2017

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-