Catalog Number

-

Brand Name

Wrist Fusion Plate, Standard Bend

Version/Model Number

WFSTD

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

K191118

Product Code

HRS

Product Code Name

Plate, Fixation, Bone

Public Device Record Key

e4fbfc99-94c4-412d-9115-761e14547b52

Public Version Date

June 26, 2020

Public Version Number

1

DI Record Publish Date

June 18, 2020

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-