Catalog Number

925.ZDK-BX12

Brand Name

Bone Foam

Version/Model Number

925.ZDK-BX12

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"

Yes

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

IQI

Product Code Name

ORTHOSIS, LIMB BRACE

Public Device Record Key

833337ad-3e4a-4a42-8ad1-0ec23079b4ea

Public Version Date

June 10, 2022

Public Version Number

2

DI Record Publish Date

May 22, 2022

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-