Catalog Number

9024-00

Brand Name

4.5mm BONE-LOK PLS Implant

Version/Model Number

LSW-45-3040

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

December 23, 2016

Issuing Agency

In GS1

MRI safety Status

MR Safe

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

-

Product Code

MRW

Product Code Name

System, Facet Screw Spinal Device

Public Device Record Key

7b7b98fe-a75f-4735-a1ae-0fc66b8e1ad9

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

September 14, 2015

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-