Catalog Number

1067716-63

Brand Name

Biomet SpinalPak Non-invasive Spine Fusion Stimulator System

Version/Model Number

1067716-63

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

P850022

Product Code

LOF

Product Code Name

Stimulator, Bone Growth, Non-Invasive

Public Device Record Key

4a2dc192-edb7-4bf2-954b-26ace6f6a5e1

Public Version Date

March 10, 2022

Public Version Number

2

DI Record Publish Date

February 28, 2019

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-