Catalog Number

CTM000758-059 TI

Brand Name

RetroFix

Version/Model Number

110L:PROX6-40L:DIST4 TI

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

K200226

Product Code

HWC

Product Code Name

Screw, Fixation, Bone

Public Device Record Key

90ccc08c-eeec-4bc0-8584-d2b14ef8b916

Public Version Date

January 07, 2021

Public Version Number

1

DI Record Publish Date

December 30, 2020

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-