Catalog Number

86000110

Brand Name

Repair bur vks-oc 2.2

Version/Model Number

86000110

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)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code

EGG

Product Code Name

ATTACHMENT, PRECISION, ALL

Public Device Record Key

269d1ef4-a051-4e4d-9e8b-8b984a1bacdd

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

September 22, 2016

Package DI Number

EBRE860001109

Quantity per Package

1

Contains DI Package

EBRE860001100

Package Discontinue Date

September 22, 2016

Package Status

Not in Commercial Distribution

Package Type

dummy