TAPERLOC COMPLETE XR 123 FEMORAL 51-105120

GUDID 00880304517134

Biomet Orthopedics, LLC

Coated hip femur prosthesis, modular
Primary Device ID00880304517134
NIH Device Record Key61e9cd67-4cb9-4e0a-bbfe-b3e20b8e8ed0
Commercial Distribution StatusIn Commercial Distribution
Brand NameTAPERLOC COMPLETE XR 123 FEMORAL
Version Model Number51-105120
Catalog Number51-105120
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
GS100880304517134 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

OQGHip Prosthesis, semi-constrained, cemented, metal/polymer, + additive, porous, uncemented

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 [TAPERLOC COMPLETE XR 123 FEMORAL]

0088030451719651-105180
0088030451718951-105170
0088030451717251-105160
0088030451716551-105150
0088030451715851-105140
0088030451714151-105130
0088030451713451-105120
0088030451712751-105110
0088030451711051-105100
0088030451710351-105090
0088030451691551-102080
0088030451690851-102070
0088030451689251-102060
0088030451688551-102050
0088030451687851-102040
0088030451722651-105240
0088030451721951-105220
0088030451720251-105200

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