Catalog Number

-

Brand Name

SIMPLANT®

Version/Model Number

54500219

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

August 13, 2020

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

-

Product Code

EBG

Product Code Name

CROWN AND BRIDGE, TEMPORARY, RESIN

Public Device Record Key

06163b0d-67f4-4efb-b5e9-ab6b5cb75439

Public Version Date

October 29, 2021

Public Version Number

5

DI Record Publish Date

March 16, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-