ORTHOLOC 3DI - WRIGHT MEDICAL TECHNOLOGY, INC.

Duns Number:807201207

Want to know more about this Product? Request more information now!


More Product Details

Catalog Number

5820X3536

Brand Name

ORTHOLOC 3DI

Version/Model Number

5820X3536

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

Product Characteristics

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 Details

Product Code

HRS

Product Code Name

Plate, fixation, bone

Device Record Status

Public Device Record Key

551fd424-65ef-4f69-9278-3426b400fd31

Public Version Date

May 26, 2022

Public Version Number

4

DI Record Publish Date

April 11, 2016

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"WRIGHT MEDICAL TECHNOLOGY, INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 1994
2 A medical device with a moderate to high risk that requires special controls. 5554