Biomet SpinalPak / OrthoPak - 20" LEAD WIRES, REPLACEMENT - EBI, LLC

Duns Number:050410323

Device Description: 20" LEAD WIRES, REPLACEMENT

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More Product Details

Catalog Number

1067724-2

Brand Name

Biomet SpinalPak / OrthoPak

Version/Model Number

1067724-2

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

Product Characteristics

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 Details

Product Code

LOF

Product Code Name

Stimulator, Bone Growth, Non-Invasive

Device Record Status

Public Device Record Key

dea071ef-d19a-4fc9-b630-4cf58e0b1cbf

Public Version Date

March 10, 2022

Public Version Number

4

DI Record Publish Date

September 19, 2014

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"EBI, LLC" Characteristics
Device Class Device Class Description No of Devices
2 A medical device with a moderate to high risk that requires special controls. 7
3 A medical device with high risk that requires premarket approval 70