FREEDOM RINGLOC HIP SYSTEM 11-107323

GUDID 00880304203730

Biomet Orthopedics, LLC

Constrained polyethylene acetabular liner
Primary Device ID00880304203730
NIH Device Record Keya614073c-d0b6-4132-a548-045eaf71c7d3
Commercial Distribution StatusIn Commercial Distribution
Brand NameFREEDOM RINGLOC HIP SYSTEM
Version Model Number11-107323
Catalog Number11-107323
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
GS100880304203730 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

KWZProsthesis, hip, constrained, cemented or uncemented, metal/polymer

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 [FREEDOM RINGLOC HIP SYSTEM]

0088030420383911-107427
0088030420382211-107426
0088030420381511-107425
0088030420380811-107424
0088030420378511-107423
0088030420377811-107327
0088030420376111-107326
0088030420375411-107325
0088030420374711-107324
0088030420373011-107323
0088030420372311-107227
0088030420371611-107226
0088030420370911-107225
0088030420369311-107224
0088030420368611-107223
0088030420367911-107222
0088030420357011-107027
0088030420356311-107026
0088030420355611-107025
0088030420354911-107024
0088030420352511-107023
0088030420350111-107022

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