Catalog Number

DF900010

Brand Name

DOLPHIX

Version/Model Number

Drill brace

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

January 01, 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

K132363

Product Code

JDW

Product Code Name

Pin, Fixation, Threaded

Public Device Record Key

d63781da-646f-48b1-b01c-0fe4d00df751

Public Version Date

September 20, 2021

Public Version Number

4

DI Record Publish Date

September 29, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-