Catalog Number

1017-0-2059

Brand Name

Consensus Hip System

Version/Model Number

1017-0-2059

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"

Yes

For Single-Use

Yes

Prescription Use (Rx)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

Yes

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

-

FDA Premarket Submission

-

Product Code

KWL

Product Code Name

Prosthesis, hip, hemi-, femoral, metal

Public Device Record Key

21a54b3a-a4b4-4d85-9b8d-d5521bec8806

Public Version Date

January 24, 2022

Public Version Number

1

DI Record Publish Date

January 15, 2022

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-