TUNNELOC® 906512

GUDID 00887868226649

Biomet Orthopedics, LLC

Tendon/ligament bone anchor, non-bioabsorbable
Primary Device ID00887868226649
NIH Device Record Key80b46af1-7a35-4b54-a4f8-f8d99e6ce41e
Commercial Distribution StatusIn Commercial Distribution
Brand NameTUNNELOC®
Version Model Number906512
Catalog Number906512
Company DUNS129278169
Company NameBiomet Orthopedics, 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
GS100887868226649 [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 Number5
Public Version Date2019-03-21
Device Publish Date2017-10-09

On-Brand Devices [TUNNELOC®]

00887868226670906515
00887868226663906514
00887868226656906513
00887868226649906512

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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