Catalog Number

176-054

Brand Name

Centerline

Version/Model Number

176-054

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

K151196

Product Code

NKB

Product Code Name

Thoracolumbosacral pedicle screw system

Public Device Record Key

5d4b0331-20f9-4395-93f1-a12f6e1a1960

Public Version Date

November 27, 2019

Public Version Number

1

DI Record Publish Date

November 19, 2019

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-