Catalog Number

E0016020-2

Brand Name

Trauma - Misc

Version/Model Number

E0016020-2

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

K123055

Product Code

HRS

Product Code Name

Plate, fixation, bone

Public Device Record Key

957f4673-4b32-4c9c-a5e8-c419175a0fc1

Public Version Date

December 07, 2018

Public Version Number

3

DI Record Publish Date

April 09, 2018

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-