LOCKING CORTICAL SCREW 815045552

GUDID 00887868040962

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 ID00887868040962
NIH Device Record Key651914ca-0e4c-46ce-a76c-10f961d9d060
Commercial Distribution StatusIn Commercial Distribution
Brand NameLOCKING CORTICAL SCREW
Version Model Number8150-45-552
Catalog Number815045552
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
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
GS100887868040962 [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

[00887868040962]

Moist Heat or Steam Sterilization


[00887868040962]

Moist Heat or Steam Sterilization


[00887868040962]

Moist Heat or Steam Sterilization


[00887868040962]

Moist Heat or Steam Sterilization


[00887868040962]

Moist Heat or Steam Sterilization


[00887868040962]

Moist Heat or Steam Sterilization


[00887868040962]

Moist Heat or Steam Sterilization


[00887868040962]

Moist Heat or Steam Sterilization


[00887868040962]

Moist Heat or Steam Sterilization


[00887868040962]

Moist Heat or Steam Sterilization


[00887868040962]

Moist Heat or Steam Sterilization


[00887868040962]

Moist Heat or Steam Sterilization


[00887868040962]

Moist Heat or Steam Sterilization


[00887868040962]

Moist Heat or Steam Sterilization


[00887868040962]

Moist Heat or Steam Sterilization


[00887868040962]

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 CORTICAL SCREW]

008878680433838161-35-075
008878680433768161-35-070
008878680433698161-35-065
008878680433528161-35-060
008878680433458161-35-058
008878680433388161-35-056
008878680433218161-35-054
008878680433148161-35-052
008878680433078161-35-050
008878680432918161-35-048
008878680432848161-35-046
008878680432778161-35-044
008878680432608161-35-042
008878680432538161-35-040
008878680432468161-35-038
008878680432398161-35-036
008878680432228161-35-034
008878680432158161-35-032
008878680432088161-35-030
00887868043192816135028
008878680431858161-35-026
008878680431788161-35-024
008878680431618161-35-022
008878680431548161-35-020
008878680431478161-35-018
008878680431308161-35-016
008878680431238161-35-014
008878680431168161-35-012
008878680431098161-35-010
008878680464698163-27-030
008878680464528163-27-028
008878680464458163-27-026
008878680464388163-27-024
008878680464218163-27-022
008878680464148163-27-020
008878680464078163-27-018
008878680463918163-27-016
008878680463848163-27-014
008878680463778163-27-012
008878680463608163-27-010
008878680465688163-27-050
008878680465518163-27-048
008878680465448163-27-046
008878680465378163-27-044
008878680465208163-27-042
008878680465138163-27-040
008878680465068163-27-038
008878680464908163-27-036
008878680464838163-27-034
008878680464768163-27-032

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