TAPERLOC COMPLETE XR 123 MICRO FEMORAL 51-145130

GUDID 00880304517325

Biomet Orthopedics, LLC

Coated hip femur prosthesis, modular
Primary Device ID00880304517325
NIH Device Record Keycee7df08-19e9-4841-a76e-5894b9bbafd2
Commercial Distribution StatusIn Commercial Distribution
Brand NameTAPERLOC COMPLETE XR 123 MICRO FEMORAL
Version Model Number51-145130
Catalog Number51-145130
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
GS100880304517325 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

LPHPROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, 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 MICRO FEMORAL]

0088030451745551-149080
0088030451744851-149070
0088030451743151-149060
0088030451742451-149050
0088030451741751-149040
0088030451737051-145180
0088030451736351-145170
0088030451735651-145160
0088030451734951-145150
0088030451733251-145140
0088030451732551-145130
0088030451731851-145120
0088030451730151-145110
0088030451729551-145100
0088030451728851-145090

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