Catalog Number

OC002A.089.032 STE

Brand Name

GUIDE PIN/SCREW

Version/Model Number

OC002A.089.032 STE

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

ebd97064-09ce-4a94-8ad3-6f04180b8325

Public Version Date

October 13, 2020

Public Version Number

1

DI Record Publish Date

October 05, 2020

Package DI Number

24053613282608

Quantity per Package

1

Contains DI Package

14053613282601

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-