LACTOSCREW 905581

GUDID 00880304453401

Biomet Sports Medicine, LLC

Tendon/ligament bone anchor, bioabsorbable
Primary Device ID00880304453401
NIH Device Record Keyf86e99c2-442a-4a1a-a7c6-f9499c29993d
Commercial Distribution StatusIn Commercial Distribution
Brand NameLACTOSCREW
Version Model Number905581
Catalog Number905581
Company DUNS627100159
Company NameBiomet Sports Medicine, 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

Device Dimensions

Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS100880304453401 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

JDRSTAPLE, 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 [LACTOSCREW]

00880304453401905581
00880304453395905580
00880304420953905572
00880304420946905571
00880304420939905570

Trademark Results [LACTOSCREW]

Mark Image

Registration | Serial
Company
Trademark
Application Date
LACTOSCREW
LACTOSCREW
76212866 2753761 Dead/Cancelled
Biomet Manufacturing Corp.
2001-02-14

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