Catalog Number

SCA-IN 40 10-S

Brand Name

SCARLET AC-T INSTRUMENTATION

Version/Model Number

SCA-IN 40 10-S

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

May 09, 2017

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

OVE

Product Code Name

Intervertebral Fusion Device With Integrated Fixation, Cervical

Public Device Record Key

8bdfc49a-43ab-4710-9ee2-146f4d50163d

Public Version Date

December 05, 2018

Public Version Number

4

DI Record Publish Date

September 27, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-