SCREW, CANCELLOUS LAG 815540100

GUDID 00887868042270

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 ID00887868042270
NIH Device Record Key4267d5a1-f49d-4e3a-9c4a-c60d0d447c68
Commercial Distribution StatusIn Commercial Distribution
Brand NameSCREW, CANCELLOUS LAG
Version Model Number8155-40-100
Catalog Number815540100
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
GS100887868042270 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

HWCScrew, fixation, bone

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00887868042270]

Moist Heat or Steam Sterilization


[00887868042270]

Moist Heat or Steam Sterilization


[00887868042270]

Moist Heat or Steam Sterilization


[00887868042270]

Moist Heat or Steam Sterilization


[00887868042270]

Moist Heat or Steam Sterilization


[00887868042270]

Moist Heat or Steam Sterilization


[00887868042270]

Moist Heat or Steam Sterilization


[00887868042270]

Moist Heat or Steam Sterilization


[00887868042270]

Moist Heat or Steam Sterilization


[00887868042270]

Moist Heat or Steam Sterilization


[00887868042270]

Moist Heat or Steam Sterilization


[00887868042270]

Moist Heat or Steam Sterilization


[00887868042270]

Moist Heat or Steam Sterilization


[00887868042270]

Moist Heat or Steam Sterilization


[00887868042270]

Moist Heat or Steam Sterilization


[00887868042270]

Moist Heat or Steam Sterilization


[00887868042270]

Moist Heat or Steam Sterilization


[00887868042270]

Moist Heat or Steam Sterilization


[00887868042270]

Moist Heat or Steam Sterilization


[00887868042270]

Moist Heat or Steam Sterilization


[00887868042270]

Moist Heat or Steam Sterilization


[00887868042270]

Moist Heat or Steam Sterilization


[00887868042270]

Moist Heat or Steam Sterilization


[00887868042270]

Moist Heat or Steam Sterilization


[00887868042270]

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 [SCREW, CANCELLOUS LAG]

008878680422708155-40-100
008878680422638155-40-095
008878680422568155-40-090
008878680422498155-40-085
008878680422328155-40-080
008878680422258155-40-075
008878680422188155-40-070
008878680422018155-40-065
008878680421958155-40-060
008878680421888155-40-055
008878680421718155-40-050
008878680421648155-40-045
008878680421578155-40-040
008878680421408155-40-035
008878680421338155-40-030
008878680421268155-40-028
008878680421198155-40-026
008878680421028155-40-024
008878680420968155-40-022
008878680420898155-40-020
008878680420728155-40-018
008878680420658155-40-016
008878680420588155-40-014

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