LOCKING CANCELLOUS SCREW 815355044

GUDID 00887868041778

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 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 ID00887868041778
NIH Device Record Keyfe5570b9-30ca-4855-9053-0e670520472f
Commercial Distribution StatusIn Commercial Distribution
Brand NameLOCKING CANCELLOUS SCREW
Version Model Number8153-55-044
Catalog Number815355044
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
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 Identifiers

Device Issuing AgencyDevice ID
GS100887868041778 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

HRSPLATE, FIXATION, BONE

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00887868041778]

Moist Heat or Steam Sterilization


[00887868041778]

Moist Heat or Steam Sterilization


[00887868041778]

Moist Heat or Steam Sterilization


[00887868041778]

Moist Heat or Steam Sterilization


[00887868041778]

Moist Heat or Steam Sterilization


[00887868041778]

Moist Heat or Steam Sterilization


[00887868041778]

Moist Heat or Steam Sterilization


[00887868041778]

Moist Heat or Steam Sterilization


[00887868041778]

Moist Heat or Steam Sterilization


[00887868041778]

Moist Heat or Steam Sterilization


[00887868041778]

Moist Heat or Steam Sterilization


[00887868041778]

Moist Heat or Steam Sterilization


[00887868041778]

Moist Heat or Steam Sterilization


[00887868041778]

Moist Heat or Steam Sterilization


[00887868041778]

Moist Heat or Steam Sterilization


[00887868041778]

Moist Heat or Steam Sterilization


[00887868041778]

Moist Heat or Steam Sterilization


[00887868041778]

Moist Heat or Steam Sterilization


[00887868041778]

Moist Heat or Steam Sterilization


[00887868041778]

Moist Heat or Steam Sterilization


[00887868041778]

Moist Heat or Steam Sterilization


[00887868041778]

Moist Heat or Steam Sterilization


[00887868041778]

Moist Heat or Steam Sterilization


[00887868041778]

Moist Heat or Steam Sterilization


[00887868041778]

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 [LOCKING CANCELLOUS SCREW]

00887868077449815355014
008878680418088153-55-048
008878680417928153-55-046
008878680417788153-55-044
008878680417618153-55-042
008878680417478153-55-038
008878680417308153-55-036
008878680417168153-55-034
008878680417098153-55-032
008878680416868153-55-028
008878680416798153-55-026
008878680416558153-55-024
008878680416488153-55-022
008878680416318153-55-020
008878680416248153-55-018
008878680416178153-55-016

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