CANNULATED CANCELLOUS SCREW 14192120

GUDID 00887868010095

Biomet Orthopedics, LLC

Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile
Primary Device ID00887868010095
NIH Device Record Keya766a98c-3750-49ac-9aaf-40fa31f8f343
Commercial Distribution StatusIn Commercial Distribution
Brand NameCANNULATED CANCELLOUS SCREW
Version Model Number14192-120
Catalog Number14192120
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

Device Dimensions

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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 Identifiers

Device Issuing AgencyDevice ID
GS100887868010095 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

LXTAPPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT, METAL COMPOSITE

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00887868010095]

Moist Heat or Steam Sterilization


[00887868010095]

Moist Heat or Steam Sterilization


[00887868010095]

Moist Heat or Steam Sterilization


[00887868010095]

Moist Heat or Steam Sterilization


[00887868010095]

Moist Heat or Steam Sterilization


[00887868010095]

Moist Heat or Steam Sterilization


[00887868010095]

Moist Heat or Steam Sterilization


[00887868010095]

Moist Heat or Steam Sterilization


[00887868010095]

Moist Heat or Steam Sterilization


[00887868010095]

Moist Heat or Steam Sterilization


[00887868010095]

Moist Heat or Steam Sterilization


[00887868010095]

Moist Heat or Steam Sterilization


[00887868010095]

Moist Heat or Steam Sterilization


[00887868010095]

Moist Heat or Steam Sterilization


[00887868010095]

Moist Heat or Steam Sterilization


[00887868010095]

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 [CANNULATED CANCELLOUS SCREW]

0088786801009514192-120
0088786801008814192-115
0088786801007114192-110
0088786801006414192-105
0088786801005714192-100
0088786800659314192-95
0088786800658614192-90
0088786800657914192-85
0088786800656214192-80
0088786800655514192-75
0088786800654814192-70
0088786800653114192-65
0088786800652414192-60
0088786800651714192-55
0088786800650014192-50
0088786800649414192-45
0088786800648714192-40
0088786800647014192-35

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