Catalog Number

-

Brand Name

Shoulder System

Version/Model Number

04.01.0284

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

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

K210207

Product Code

MBF

Product Code Name

Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer, Uncemented

Public Device Record Key

7878694c-352f-4b7e-b33b-1d9490f5628e

Public Version Date

April 06, 2021

Public Version Number

1

DI Record Publish Date

March 29, 2021

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-