G7 FINNED ACETABULAR SHELL 110017116

GUDID 00880304672239

Biomet Orthopedics, LLC

Non-constrained polyethylene acetabular liner
Primary Device ID00880304672239
NIH Device Record Keyf664a912-3e41-450e-b869-d8bcf2f74ca3
Commercial Distribution StatusIn Commercial Distribution
Brand NameG7 FINNED ACETABULAR SHELL
Version Model Number110017116
Catalog Number110017116
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 Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
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

Device Dimensions

Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS100880304672239 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

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

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-05-08
Device Publish Date2020-04-30

On-Brand Devices [G7 FINNED ACETABULAR SHELL]

00880304672185110017111
00880304672178110017110
00880304672161110017109
00880304672154110017108
00880304672147110017107
00880304672130110017106
00880304672123110017105
00880304672116110017104
00880304672109110017103
00880304672093110017102
00880304672086110017101
00880304672079110017100
00880304672062110017099
00880304672055110017098
00880304672246110017117
00880304672239110017116
00880304672222110017115
00880304672215110017114
00880304672208110017113
00880304672192110017112

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