Catalog Number

-

Brand Name

IO FiX

Version/Model Number

118-20006

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

K150309

Product Code

HRS

Product Code Name

Plate, Fixation, Bone

Public Device Record Key

04078cb7-25c5-47ea-8c62-b49d63672f38

Public Version Date

July 05, 2019

Public Version Number

1

DI Record Publish Date

June 27, 2019

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-