Catalog Number

-

Brand Name

BLACKBIRD™ Spinal System

Version/Model Number

L070-0021

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

K133214

Product Code

HXW

Product Code Name

BENDER

Public Device Record Key

d74f403f-fdbd-4f90-b384-a449167b8684

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

March 18, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-