MALLORY/HEAD INTERLOK HIP SYSTEM 105613

GUDID 00880304007222

Biomet Orthopedics, LLC

Uncoated hip femur prosthesis, modular
Primary Device ID00880304007222
NIH Device Record Key24a38a6f-8199-40e4-88b4-379ff0ff66fe
Commercial Distribution StatusIn Commercial Distribution
Brand NameMALLORY/HEAD INTERLOK HIP SYSTEM
Version Model Number105613
Catalog Number105613
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 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
GS100880304007222 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

JDIProsthesis, hip, semi-constrained, metal/polymer, cemented

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

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

On-Brand Devices [MALLORY/HEAD INTERLOK HIP SYSTEM]

00880304192133105615
00880304192102105611
00880304192072105607
00880304192058105606
00880304007222105613
00880304007208105609

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