Catalog Number

KWDT-1520/5

Brand Name

FO Micro Screw System

Version/Model Number

KWDT-1520

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

K180348,K180348

Product Code

HTY

Product Code Name

Pin, Fixation, Smooth

Public Device Record Key

de18ba6c-d8db-4ee0-90ea-3b8f53099f4d

Public Version Date

February 21, 2019

Public Version Number

1

DI Record Publish Date

January 21, 2019

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-