Catalog Number

1067723

Brand Name

Biomet SpinalPak / OrthoPak

Version/Model Number

1067723

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

P850022

Product Code

LOF

Product Code Name

Stimulator, Bone Growth, Non-Invasive

Public Device Record Key

96940aa4-3082-4311-a771-fdd97b39f3f1

Public Version Date

March 10, 2022

Public Version Number

4

DI Record Publish Date

September 19, 2014

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-