Catalog Number

56-17004

Brand Name

AXS

Version/Model Number

56-17004

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

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

K172572,K172572

Product Code

JEY

Product Code Name

PLATE, BONE

Public Device Record Key

43c9f612-95db-4565-a938-ef3a9654143d

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

November 18, 2017

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-