Arcos® Modular Revision System 31-301325

GUDID 00887868476587

Biomet Orthopedics, LLC

Femoral stem prosthesis trial Femoral stem prosthesis trial Femoral stem prosthesis trial Femoral stem prosthesis trial Femoral stem prosthesis trial Femoral stem prosthesis trial Femoral stem prosthesis trial Femoral stem prosthesis trial Femoral stem prosthesis trial Femoral stem prosthesis trial Femoral stem prosthesis trial Femoral stem prosthesis trial
Primary Device ID00887868476587
NIH Device Record Keycc71ce89-8d4d-4424-befa-7efc13083760
Commercial Distribution StatusIn Commercial Distribution
Brand NameArcos® Modular Revision System
Version Model Number31-301325
Catalog Number31-301325
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

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 Identifiers

Device Issuing AgencyDevice ID
GS100887868476587 [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

[00887868476587]

Moist Heat or Steam Sterilization


[00887868476587]

Moist Heat or Steam Sterilization


[00887868476587]

Moist Heat or Steam Sterilization


[00887868476587]

Moist Heat or Steam Sterilization


[00887868476587]

Moist Heat or Steam Sterilization


[00887868476587]

Moist Heat or Steam Sterilization


[00887868476587]

Moist Heat or Steam Sterilization


[00887868476587]

Moist Heat or Steam Sterilization


[00887868476587]

Moist Heat or Steam Sterilization


[00887868476587]

Moist Heat or Steam Sterilization


[00887868476587]

Moist Heat or Steam Sterilization


[00887868476587]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-05-16
Device Publish Date2022-05-08

On-Brand Devices [Arcos® Modular Revision System]

0088786847862831-311355
0088786847861131-311354
0088786847860431-311353
0088786847859831-311352
0088786847858131-311351
0088786847857431-311345
0088786847856731-311344
0088786847855031-311343
0088786847854331-311342
0088786847853631-311341
0088786847852931-311335
0088786847851231-311334
0088786847850531-311333
0088786847849931-311332
0088786847848231-311331
0088786847847531-311325
0088786847846831-311324
0088786847845131-311323
0088786847844431-311322
0088786847843731-311321
0088786847842031-311315
0088786847841331-311314
0088786847840631-311313
0088786847839031-311312
0088786847838331-311311
0088786847837631-311310
0088786847836931-311305
0088786847835231-311304
0088786847834531-311303
0088786847833831-311302
0088786847832131-311301
0088786847831431-311300
0088786847830731-311000
0088786847807931-301890
0088786847627331-301110
0088786847626631-301109
0088786847625931-301107
0088786847623531-301105
0088786847622831-301104
0088786847621131-301103
0088786847787431-301843
0088786847786731-301842
0088786847785031-301841
0088786847784331-301840
0088786847783631-301839
0088786847782931-301838
0088786847781231-301837
0088786847780531-301836
0088786847779931-301835
0088786847778231-301834

Trademark Results [Arcos]

Mark Image

Registration | Serial
Company
Trademark
Application Date
ARCOS
ARCOS
98001041 not registered Live/Pending
HLI Solutions, Inc.
2023-05-17
ARCOS
ARCOS
97567037 not registered Live/Pending
Siman, Alvaro E.
2022-08-26
ARCOS
ARCOS
97141919 not registered Live/Pending
Hubbell Lighting, Inc.
2021-11-24
ARCOS
ARCOS
88750745 not registered Live/Pending
Arcos, Inc.
2020-01-08
ARCOS
ARCOS
88500444 not registered Live/Pending
Archimedes Controls Corp.
2019-07-03
ARCOS
ARCOS
87601803 5577107 Live/Registered
Arrcus, Inc.
2017-09-08
ARCOS
ARCOS
87588350 not registered Dead/Abandoned
SCOPERTA IMPORTING COMPANY
2017-08-29
ARCOS
ARCOS
86823144 5392314 Live/Registered
Dosamar Corporation
2015-11-17
ARCOS
ARCOS
86114301 not registered Dead/Abandoned
Smith, Logan
2013-11-08
ARCOS
ARCOS
85801573 4379613 Live/Registered
ARCOS, LLC
2012-12-13
ARCOS
ARCOS
85801564 4379612 Live/Registered
ARCOS, LLC
2012-12-13
ARCOS
ARCOS
85801551 4570680 Live/Registered
ARCOS, INC.
2012-12-13

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