Catalog Number

5407-150-000

Brand Name

NA

Version/Model Number

5407-150-000

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

DZJ

Product Code Name

DRIVER, WIRE, AND BONE DRILL, MANUAL

Public Device Record Key

6bbb7e03-dac9-4a12-944a-e1f17d431c5b

Public Version Date

June 10, 2022

Public Version Number

4

DI Record Publish Date

July 08, 2021

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-