Catalog Number

-

Brand Name

ARUM NB 1 SA Fixture

Version/Model Number

NB14007SP

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

K213506

Product Code

DZE

Product Code Name

Implant, Endosseous, Root-Form

Public Device Record Key

cf6bd076-2e68-40d9-9e4a-df27eed4f08c

Public Version Date

July 11, 2022

Public Version Number

2

DI Record Publish Date

June 08, 2022

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-