CANNULATED FULLY THREADED CANCELLOUS SCREWREDUCED HEAD 180248010

GUDID 00887868017667

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 ID00887868017667
NIH Device Record Keyfc1698c0-1035-49ec-bf3f-4b24c1e6306b
Commercial Distribution StatusIn Commercial Distribution
Brand NameCANNULATED FULLY THREADED CANCELLOUS SCREWREDUCED HEAD
Version Model Number1802-48-010
Catalog Number180248010
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

Device Size Text, specify0
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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 Identifiers

Device Issuing AgencyDevice ID
GS100887868017667 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

HTYPIN, FIXATION, SMOOTH

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00887868017667]

Moist Heat or Steam Sterilization


[00887868017667]

Moist Heat or Steam Sterilization


[00887868017667]

Moist Heat or Steam Sterilization


[00887868017667]

Moist Heat or Steam Sterilization


[00887868017667]

Moist Heat or Steam Sterilization


[00887868017667]

Moist Heat or Steam Sterilization


[00887868017667]

Moist Heat or Steam Sterilization


[00887868017667]

Moist Heat or Steam Sterilization


[00887868017667]

Moist Heat or Steam Sterilization


[00887868017667]

Moist Heat or Steam Sterilization


[00887868017667]

Moist Heat or Steam Sterilization


[00887868017667]

Moist Heat or Steam Sterilization


[00887868017667]

Moist Heat or Steam Sterilization


[00887868017667]

Moist Heat or Steam Sterilization


[00887868017667]

Moist Heat or Steam Sterilization


[00887868017667]

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 FULLY THREADED CANCELLOUS SCREWREDUCED HEAD]

008878680179021802-48-070
008878680178961802-48-065
008878680178891802-48-060
008878680178721802-48-055
008878680178651802-48-050
008878680178581802-48-048
008878680178411802-48-046
008878680178341802-48-044
008878680178271802-48-042
008878680178101802-48-040
008878680178031802-48-038
008878680177971802-48-036
008878680177801802-48-034
008878680177731802-48-032
008878680177661802-48-030
008878680177591802-48-028
008878680177421802-48-026
008878680177351802-48-024
008878680177281802-48-022
008878680177111802-48-020
008878680177041802-48-018
008878680176981802-48-016
008878680176811802-48-014
008878680176741802-48-012
008878680176671802-48-010

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