VISION FOOTRING 21202

GUDID 00887868151194

Biomet Orthopedics, LLC

External orthopaedic fixation system, single-use, non-sterile
Primary Device ID00887868151194
NIH Device Record Keya270e783-4477-48c4-b3c0-1bd00d8634dd
Commercial Distribution StatusIn Commercial Distribution
Brand NameVISION FOOTRING
Version Model Number21202
Catalog Number21202
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 Dimensions

Device Size Text, specify0
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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
GS100887868151194 [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

[00887868151194]

Moist Heat or Steam Sterilization


[00887868151194]

Moist Heat or Steam Sterilization


[00887868151194]

Moist Heat or Steam Sterilization


[00887868151194]

Moist Heat or Steam Sterilization


[00887868151194]

Moist Heat or Steam Sterilization


[00887868151194]

Moist Heat or Steam Sterilization


[00887868151194]

Moist Heat or Steam Sterilization


[00887868151194]

Moist Heat or Steam Sterilization


[00887868151194]

Moist Heat or Steam Sterilization


[00887868151194]

Moist Heat or Steam Sterilization


[00887868151194]

Moist Heat or Steam Sterilization


[00887868151194]

Moist Heat or Steam Sterilization


[00887868151194]

Moist Heat or Steam Sterilization


[00887868151194]

Moist Heat or Steam Sterilization


[00887868151194]

Moist Heat or Steam Sterilization


[00887868151194]

Moist Heat or Steam Sterilization


[00887868151194]

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]

0088786815123121212
0088786815122421210
0088786815121721207
0088786815120021205
0088786815119421202
0088786815118721200

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