CANCELLOUS LAG SCREW 855540095

GUDID 00887868059902

Biomet Orthopedics, LLC

Orthopaedic bone screw, non-bioabsorbable, sterile
Primary Device ID00887868059902
NIH Device Record Keya7298a86-8559-4c99-a0b7-c6c418af878d
Commercial Distribution StatusIn Commercial Distribution
Brand NameCANCELLOUS LAG SCREW
Version Model Number8555-40-095
Catalog Number855540095
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 Datetrue
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
Device Size Text, specify0
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Device Size Text, specify0
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
GS100887868059902 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

HTNWASHER, BOLT NUT

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

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 [CANCELLOUS LAG SCREW]

0088786801056914522-120
0088786801055214522-115
0088786801054514522-110
0088786801053814522-105
0088786801052114522-100
0088786800972314522-95
0088786800971614522-90
0088786800970914522-85
0088786800969314522-80
0088786800968614522-75
0088786800967914522-70
0088786800966214522-65
0088786800965514522-60
0088786800964814522-55
0088786800963114522-50
0088786800962414522-45
0088786800961714522-40
008878680599198555-40-100
008878680599028555-40-095
008878680598968555-40-090
008878680598898555-40-085
008878680598728555-40-080
008878680598658555-40-075
008878680598588555-40-070
008878680598418555-40-065
008878680598348555-40-060
008878680598278555-40-055
008878680598108555-40-050
008878680598038555-40-045
008878680597978555-40-040
008878680597808555-40-035
008878680597738555-40-030
008878680597668555-40-028
008878680597598555-40-026
008878680597428555-40-024
008878680597358555-40-022
008878680597288555-40-020
008878680597118555-40-018
008878680597048555-40-016
008878680596988555-40-014
008878684520488555-40-070
008878684520318555-40-065
008878684520248555-40-060
008878684520178555-40-055
008878684520008555-40-050
008878684519978555-40-045
008878684519808555-40-040
008878684519738555-40-035
008878684519668555-40-030
008878684519598555-40-028

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