OSS™ TIBIAL BEARING PROVISIONAL 32-472050

GUDID 00887868458637

Biomet Orthopedics, LLC

Knee tibia prosthesis trial Knee tibia prosthesis trial Knee tibia prosthesis trial, reusable Knee tibia prosthesis trial, reusable Knee tibia prosthesis trial, reusable Knee tibia prosthesis trial, reusable Knee tibia prosthesis trial, reusable Knee tibia prosthesis trial, reusable Knee tibia prosthesis trial, reusable Knee tibia prosthesis trial, reusable Knee tibia prosthesis trial, reusable Knee tibia prosthesis trial, reusable Knee tibia prosthesis trial, reusable Knee tibia prosthesis trial, reusable Knee tibia prosthesis trial, reusable Knee tibia prosthesis trial, reusable Knee tibia prosthesis trial, reusable Knee tibia prosthesis trial, reusable Knee tibia prosthesis trial, reusable Knee tibia prosthesis trial, reusable Knee tibia prosthesis trial, reusable Knee tibia prosthesis trial, reusable Knee tibia prosthesis trial, reusable Knee tibia prosthesis trial, reusable Knee tibia prosthesis trial, reusable Knee tibia prosthesis trial, reusable Knee tibia prosthesis trial, reusable Knee tibia prosthesis trial, reusable Knee tibia prosthesis trial, reusable Knee tibia prosthesis trial, reusable
Primary Device ID00887868458637
NIH Device Record Key8c5826c0-b5e1-4d4f-8254-4e604cb2279b
Commercial Distribution StatusIn Commercial Distribution
Brand NameOSS™ TIBIAL BEARING PROVISIONAL
Version Model Number32-472050
Catalog Number32-472050
Company DUNS129278169
Company NameBiomet Orthopedics, LLC
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com

Device Dimensions

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Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
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Device Size Text, specify0
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Device Identifiers

Device Issuing AgencyDevice ID
GS100887868458637 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

JDIProsthesis, hip, semi-constrained, metal/polymer, cemented

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00887868458637]

Moist Heat or Steam Sterilization


[00887868458637]

Moist Heat or Steam Sterilization


[00887868458637]

Moist Heat or Steam Sterilization


[00887868458637]

Moist Heat or Steam Sterilization


[00887868458637]

Moist Heat or Steam Sterilization


[00887868458637]

Moist Heat or Steam Sterilization


[00887868458637]

Moist Heat or Steam Sterilization


[00887868458637]

Moist Heat or Steam Sterilization


[00887868458637]

Moist Heat or Steam Sterilization


[00887868458637]

Moist Heat or Steam Sterilization


[00887868458637]

Moist Heat or Steam Sterilization


[00887868458637]

Moist Heat or Steam Sterilization


[00887868458637]

Moist Heat or Steam Sterilization


[00887868458637]

Moist Heat or Steam Sterilization


[00887868458637]

Moist Heat or Steam Sterilization


[00887868458637]

Moist Heat or Steam Sterilization


[00887868458637]

Moist Heat or Steam Sterilization


[00887868458637]

Moist Heat or Steam Sterilization


[00887868458637]

Moist Heat or Steam Sterilization


[00887868458637]

Moist Heat or Steam Sterilization


[00887868458637]

Moist Heat or Steam Sterilization


[00887868458637]

Moist Heat or Steam Sterilization


[00887868458637]

Moist Heat or Steam Sterilization


[00887868458637]

Moist Heat or Steam Sterilization


[00887868458637]

Moist Heat or Steam Sterilization


[00887868458637]

Moist Heat or Steam Sterilization


[00887868458637]

Moist Heat or Steam Sterilization


[00887868458637]

Moist Heat or Steam Sterilization


[00887868458637]

Moist Heat or Steam Sterilization


[00887868458637]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-10-19
Device Publish Date2020-10-09

On-Brand Devices [OSS™ TIBIAL BEARING PROVISIONAL]

0088786845864432-472051
0088786845863732-472050
0088786845862032-472049
0088786845861332-472048
0088786845860632-472047
0088786845859032-472046

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