VISION FOOTRING SYSTEM 21260

GUDID 00888480221487

Biomet Orthopedics, LLC

External orthopaedic fixation system, single-use, non-sterile
Primary Device ID00888480221487
NIH Device Record Key02f82ce6-99ba-4099-b50f-abad86e43e24
Commercial Distribution StatusIn Commercial Distribution
Brand NameVISION FOOTRING SYSTEM
Version Model Number21260
Catalog Number21260
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 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

Device Identifiers

Device Issuing AgencyDevice ID
GS100888480221487 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

KTTAPPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00888480221487]

Moist Heat or Steam Sterilization


[00888480221487]

Moist Heat or Steam Sterilization


[00888480221487]

Moist Heat or Steam Sterilization


[00888480221487]

Moist Heat or Steam Sterilization


[00888480221487]

Moist Heat or Steam Sterilization


[00888480221487]

Moist Heat or Steam Sterilization


[00888480221487]

Moist Heat or Steam Sterilization


[00888480221487]

Moist Heat or Steam Sterilization


[00888480221487]

Moist Heat or Steam Sterilization


[00888480221487]

Moist Heat or Steam Sterilization


[00888480221487]

Moist Heat or Steam Sterilization


[00888480221487]

Moist Heat or Steam Sterilization


[00888480221487]

Moist Heat or Steam Sterilization


[00888480221487]

Moist Heat or Steam Sterilization


[00888480221487]

Moist Heat or Steam Sterilization


[00888480221487]

Moist Heat or Steam Sterilization


[00888480221487]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2015-10-24

On-Brand Devices [VISION FOOTRING SYSTEM]

0088030428278021415
0088786810626221430
0088786810625521425
0088786810624821395
0088786810623121235
0088848022256921446
0088848022250721444
0088848022230921442
0088848022222421440
0088848022208821410
0088848022204021405
0088848022202621400
0088848022152421270
0088848022148721260
0088848022139521245
0088848022138821244
0088848022137121243
0088848022136421242
0088848022135721240
0088848022129621225

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