Catalog Number

800-02-503

Brand Name

GUIDE PIN/SCREW

Version/Model Number

800-02-503

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

Yes

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

K131264,K131264,K131264

Product Code

HWC

Product Code Name

Screw, Fixation, Bone

Public Device Record Key

3495fac8-1b19-48bb-aae0-c7df5074503c

Public Version Date

October 05, 2020

Public Version Number

1

DI Record Publish Date

September 25, 2020

Package DI Number

24053613279660

Quantity per Package

3

Contains DI Package

14053613279663

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-