Catalog Number

110035368

Brand Name

BIOMET® BONE CEMENT R

Version/Model Number

110035368

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

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

K172408

Product Code

LOD

Product Code Name

BONE CEMENT

Public Device Record Key

e1aea920-9780-4f5f-b9a1-cd80e09c08e0

Public Version Date

June 19, 2020

Public Version Number

3

DI Record Publish Date

April 04, 2018

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-