HYBRID(TM) GLENOID 406114

GUDID 00880304456341

Biomet Orthopedics, LLC

Humeral head prosthesis trial, reusable Pure wool pillow Pure wool pillow Pure wool pillow Pure wool pillow Pure wool pillow Pure wool pillow Pure wool pillow Pure wool pillow Pure wool pillow Pure wool pillow Pure wool pillow Pure wool pillow Pure wool pillow Pure wool pillow Pure wool pillow Pure wool pillow Pure wool pillow
Primary Device ID00880304456341
NIH Device Record Key4e8c75b9-053e-4564-b6b2-1d7688fb5884
Commercial Distribution StatusIn Commercial Distribution
Brand NameHYBRID(TM) GLENOID
Version Model Number406114
Catalog Number406114
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

Device Dimensions

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

Device Identifiers

Device Issuing AgencyDevice ID
GS100880304456341 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

KWSPROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00880304456341]

Moist Heat or Steam Sterilization


[00880304456341]

Moist Heat or Steam Sterilization


[00880304456341]

Moist Heat or Steam Sterilization


[00880304456341]

Moist Heat or Steam Sterilization


[00880304456341]

Moist Heat or Steam Sterilization


[00880304456341]

Moist Heat or Steam Sterilization


[00880304456341]

Moist Heat or Steam Sterilization


[00880304456341]

Moist Heat or Steam Sterilization


[00880304456341]

Moist Heat or Steam Sterilization


[00880304456341]

Moist Heat or Steam Sterilization


[00880304456341]

Moist Heat or Steam Sterilization


[00880304456341]

Moist Heat or Steam Sterilization


[00880304456341]

Moist Heat or Steam Sterilization


[00880304456341]

Moist Heat or Steam Sterilization


[00880304456341]

Moist Heat or Steam Sterilization


[00880304456341]

Moist Heat or Steam Sterilization


[00880304456341]

Moist Heat or Steam Sterilization


[00880304456341]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2019-02-07
Device Publish Date2017-03-20

On-Brand Devices [HYBRID(TM) GLENOID]

00880304456358406112
00880304456341406114
00880304456334406113

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.