Catalog Number

-

Brand Name

Jones-FX Jones Fracture System

Version/Model Number

JC6555

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

December 29, 2017

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)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code

HWC

Product Code Name

Screw, Fixation, Bone

Public Device Record Key

609fc615-5be3-492a-913f-b98dace23f6e

Public Version Date

December 15, 2020

Public Version Number

3

DI Record Publish Date

October 17, 2015

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-