Catalog Number

-

Brand Name

Axle Interspinous Fusion System

Version/Model Number

C060-0092

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

-

Product Code

GDI

Product Code Name

DISSECTOR, SURGICAL, GENERAL & PLASTIC SURGERY

Public Device Record Key

2ae8adad-e1bd-41b2-939c-ec087dfdaf6c

Public Version Date

June 03, 2021

Public Version Number

4

DI Record Publish Date

February 23, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-