TUNNELOC 906512

GUDID 00880304516687

Biomet Sports Medicine, LLC

Tendon/ligament bone anchor, non-bioabsorbable
Primary Device ID00880304516687
NIH Device Record Key2eb97240-2be5-437d-8e5b-ea1793fa0268
Commercial Distribution StatusIn Commercial Distribution
Brand NameTUNNELOC
Version Model Number906512
Catalog Number906512
Company DUNS627100159
Company NameBiomet Sports Medicine, LLC
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Safe
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 Dimensions

Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS100880304516687 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

HWCScrew, fixation, bone

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number5
Public Version Date2019-03-21
Device Publish Date2015-10-24

On-Brand Devices [TUNNELOC]

00880304516779906515
00880304516755906514
00880304516748906513
00880304516687906512

Trademark Results [TUNNELOC]

Mark Image

Registration | Serial
Company
Trademark
Application Date
TUNNELOC
TUNNELOC
74528564 2034116 Live/Registered
BIOMET U.S. RECONSTRUCTION, LLC
1994-05-24

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