RC ARTHRORIVET 905802

GUDID 00880304421264

Biomet Sports Medicine, LLC

Tendon/ligament bone anchor, bioabsorbable
Primary Device ID00880304421264
NIH Device Record Key0b4abe35-a707-4706-9363-8c287533ced9
Commercial Distribution StatusIn Commercial Distribution
Brand NameRC ARTHRORIVET
Version Model Number905802
Catalog Number905802
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 Identifiers

Device Issuing AgencyDevice ID
GS100880304421264 [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

Devices Manufactured by Biomet Sports Medicine, LLC

00880304460454 - MAXFIRE2020-05-06
00880304475915 - MAXFIRE MARXMEN2020-05-06
00880304475922 - MAXFIRE MARXMEN2020-05-06
00880304477193 - JUGGERKNOT SOFT ANCHORS2020-02-06
00880304477315 - JUGGERKNOT SOFT ANCHORS2020-02-06
00880304508590 - JUGGERKNOT SOFT ANCHORS2020-02-06
00880304509627 - JUGGERKNOT SOFT ANCHORS2020-02-06
00880304511699 - JUGGERKNOT SOFT ANCHORS2020-02-06

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.