Catalog Number

06.6634B

Brand Name

Dymaxeon®

Version/Model Number

05.5

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

May 14, 2016

Issuing Agency

In GS1

MRI safety Status

MR Conditional

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

MNH

Product Code Name

Orthosis, spondylolisthesis spinal fixation

Public Device Record Key

9bcbd6e9-0bb4-4956-b43e-3a830fc43a23

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

January 21, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-