Catalog Number

00505301900

Brand Name

NA

Version/Model Number

5053-19

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

HTZ

Product Code Name

INSTRUMENT, CUTTING, ORTHOPEDIC

Public Device Record Key

6cfe5a9b-0cf6-43be-aa12-ec434b1f7338

Public Version Date

October 28, 2022

Public Version Number

2

DI Record Publish Date

October 05, 2021

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-