MULTI-AXIAL CORRECTION SYSTEM 15270

GUDID 00880304487406

Biomet Orthopedics, LLC

External orthopaedic fixation system, single-use, non-sterile
Primary Device ID00880304487406
NIH Device Record Key45c952a0-b04d-4ff1-baa2-42f532f4c12a
Commercial Distribution StatusIn Commercial Distribution
Brand NameMULTI-AXIAL CORRECTION SYSTEM
Version Model Number15270
Catalog Number15270
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
GS100880304487406 [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

[00880304487406]

Moist Heat or Steam Sterilization


[00880304487406]

Moist Heat or Steam Sterilization


[00880304487406]

Moist Heat or Steam Sterilization


[00880304487406]

Moist Heat or Steam Sterilization


[00880304487406]

Moist Heat or Steam Sterilization


[00880304487406]

Moist Heat or Steam Sterilization


[00880304487406]

Moist Heat or Steam Sterilization


[00880304487406]

Moist Heat or Steam Sterilization


[00880304487406]

Moist Heat or Steam Sterilization


[00880304487406]

Moist Heat or Steam Sterilization


[00880304487406]

Moist Heat or Steam Sterilization


[00880304487406]

Moist Heat or Steam Sterilization


[00880304487406]

Moist Heat or Steam Sterilization


[00880304487406]

Moist Heat or Steam Sterilization


[00880304487406]

Moist Heat or Steam Sterilization


[00880304487406]

Moist Heat or Steam Sterilization


[00880304487406]

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 [MULTI-AXIAL CORRECTION SYSTEM]

0088030455224113050
0088030451000513020
0088030449275215219
0088030449179313035
0088030449173113080
0088030449170013040
0088030449073415210
0088030448953015220
0088030448740615270
0088030448629415255
0088848019051615305
0088848019048615290
0088848019045515277
0088848019043115272
0088848019037015260
0088848019035615250
0088848019032515240
0088848015299613005
0088786809306714-415355
0088786809305014-415286
0088848044437414-415345

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