Catalog Number

MPE0-E129

Brand Name

4CIS® Marlin ACIF Cage SYSTEM

Version/Model Number

MPE0-E129

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

December 28, 2018

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

K162402

Product Code

ODP

Product Code Name

Intervertebral Fusion Device With Bone Graft, Cervical

Public Device Record Key

b36faed4-edae-44a7-96e4-5731d911a9fc

Public Version Date

March 28, 2022

Public Version Number

5

DI Record Publish Date

January 11, 2018

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-