Catalog Number

JUL-IN 19 10-N

Brand Name

JULIET INSTRUMENTATION

Version/Model Number

JUL-IN 19 10-N

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

February 05, 2019

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

-

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

MAX

Product Code Name

Intervertebral Fusion Device With Bone Graft, Lumbar

Public Device Record Key

1199c075-0baf-40d0-97f0-d32d3629f070

Public Version Date

June 10, 2022

Public Version Number

6

DI Record Publish Date

February 08, 2018

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-