ZIPTIGHT FIXATION SYSTEM 904759

GUDID 00880304476103

Biomet Orthopedics, LLC

Ligament bone anchor
Primary Device ID00880304476103
NIH Device Record Key8f8f4f83-445f-4eb3-96ec-445acd008914
Commercial Distribution StatusIn Commercial Distribution
Brand NameZIPTIGHT FIXATION SYSTEM
Version Model Number904759
Catalog Number904759
Company DUNS129278169
Company NameBiomet Orthopedics, LLC
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Conditional
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

Device Identifiers

Device Issuing AgencyDevice ID
GS100880304476103 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

MBIFASTENER, FIXATION, NONDEGRADABLE, SOFT TISSUE

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2019-01-08
Device Publish Date2015-10-24

On-Brand Devices [ZIPTIGHT FIXATION SYSTEM]

00880304476103904759
00880304476097909853
00880304475854909857
00880304473560909856

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