VISION FOOTRING SYSTEM 21425

GUDID 00887868106255

Biomet Orthopedics, LLC

External orthopaedic fixation system, single-use, sterile
Primary Device ID00887868106255
NIH Device Record Key2a0c77dc-0f5f-4fab-ac29-9a685dec7b79
Commercial Distribution StatusIn Commercial Distribution
Brand NameVISION FOOTRING SYSTEM
Version Model Number21425
Catalog Number21425
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
GS100887868106255 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

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

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

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.