Catalog Number

-

Brand Name

K-Wire with stop 1.0mm

Version/Model Number

20666

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In HIBCC

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

K162674

Product Code

LRN

Product Code Name

Wire, Surgical

Public Device Record Key

e227f126-0a1a-400c-b99c-7e115417fbc7

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

August 13, 2017

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-