Catalog Number

260520

Brand Name

Universal 2™ Total Wrist Implant System

Version/Model Number

260520

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

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

HWD

Product Code Name

STARTER, BONE SCREW

Public Device Record Key

48d08580-df21-40ed-abb1-f4afd0f378e5

Public Version Date

March 04, 2021

Public Version Number

2

DI Record Publish Date

March 09, 2018

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-