Catalog Number

FX-HL-7096

Brand Name

FuzeFix™ Large

Version/Model Number

FX-HL-7096

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

K170038

Product Code

HWC

Product Code Name

Screw, Fixation, Bone

Public Device Record Key

076d8bc1-fabf-4fa6-b224-182925d10e26

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

November 13, 2017

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-