BALL JOINT WITH ROD A11

GUDID 00887868070310

Biomet Orthopedics, LLC

External orthopaedic fixation system, single-use, non-sterile
Primary Device ID00887868070310
NIH Device Record Key3b7759d3-30a4-4f75-a261-f59585d342b1
Commercial Distribution StatusIn Commercial Distribution
Brand NameBALL JOINT WITH ROD
Version Model NumberA11
Catalog NumberA11
Company DUNS129278169
Company NameBiomet Orthopedics, 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 Datefalse
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
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100887868070310 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

JECCOMPONENT, TRACTION, INVASIVE

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00887868070310]

Moist Heat or Steam Sterilization


[00887868070310]

Moist Heat or Steam Sterilization


[00887868070310]

Moist Heat or Steam Sterilization


[00887868070310]

Moist Heat or Steam Sterilization


[00887868070310]

Moist Heat or Steam Sterilization


[00887868070310]

Moist Heat or Steam Sterilization


[00887868070310]

Moist Heat or Steam Sterilization


[00887868070310]

Moist Heat or Steam Sterilization


[00887868070310]

Moist Heat or Steam Sterilization


[00887868070310]

Moist Heat or Steam Sterilization


[00887868070310]

Moist Heat or Steam Sterilization


[00887868070310]

Moist Heat or Steam Sterilization


[00887868070310]

Moist Heat or Steam Sterilization


[00887868070310]

Moist Heat or Steam Sterilization


[00887868070310]

Moist Heat or Steam Sterilization


[00887868070310]

Moist Heat or Steam Sterilization


[00887868070310]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2015-10-24

Devices Manufactured by Biomet Orthopedics, LLC

00889024674288 - HAMMR™2024-07-03
00887868555732 - Patient Specific Planning Solution™2024-06-25
00880304658462 - Compress®2024-05-24
00889024663794 - HAMMR™2024-05-17
00889024663800 - HAMMR™2024-05-17
00889024663817 - HAMMR™2024-05-17
00889024663824 - HAMMR™2024-05-17
00889024663831 - HAMMR™2024-05-17

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