Catalog Number

60.333.120

Brand Name

Cannulated Screw System +

Version/Model Number

60.333.120

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

PXV

Product Code Name

General purpose instrument tray

Public Device Record Key

e0385c60-bb8d-483b-95c3-1d5b62af916c

Public Version Date

September 16, 2022

Public Version Number

6

DI Record Publish Date

May 21, 2020

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-