Modular Hybrid Glenoid 406152

GUDID 00887868242601

Biomet Orthopedics, LLC

Wire cutter Glenoid orthopaedic reamer Glenoid orthopaedic reamer Glenoid orthopaedic reamer Glenoid orthopaedic reamer Glenoid orthopaedic reamer Glenoid orthopaedic reamer Glenoid orthopaedic reamer Glenoid orthopaedic reamer Glenoid orthopaedic reamer Glenoid orthopaedic reamer Glenoid orthopaedic reamer Glenoid orthopaedic reamer Glenoid orthopaedic reamer
Primary Device ID00887868242601
NIH Device Record Key10f1b1f2-05a9-4aee-b381-f278238fe16e
Commercial Distribution StatusIn Commercial Distribution
Brand NameModular Hybrid Glenoid
Version Model Number406152
Catalog Number406152
Company DUNS129278169
Company NameBiomet Orthopedics, LLC
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
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

Device Identifiers

Device Issuing AgencyDevice ID
GS100887868242601 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

KWTPROSTHESIS, SHOULDER, NON-CONSTRAINED, METAL/POLYMER CEMENTED
LXHORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00887868242601]

Moist Heat or Steam Sterilization


[00887868242601]

Moist Heat or Steam Sterilization


[00887868242601]

Moist Heat or Steam Sterilization


[00887868242601]

Moist Heat or Steam Sterilization


[00887868242601]

Moist Heat or Steam Sterilization


[00887868242601]

Moist Heat or Steam Sterilization


[00887868242601]

Moist Heat or Steam Sterilization


[00887868242601]

Moist Heat or Steam Sterilization


[00887868242601]

Moist Heat or Steam Sterilization


[00887868242601]

Moist Heat or Steam Sterilization


[00887868242601]

Moist Heat or Steam Sterilization


[00887868242601]

Moist Heat or Steam Sterilization


[00887868242601]

Moist Heat or Steam Sterilization


[00887868242601]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2018-08-23
Device Publish Date2018-07-23

On-Brand Devices [Modular Hybrid Glenoid]

00887868242601406152
00887868242595406151
00887868242588406150
00887868232022SSI000928
00887868232015SSI000927
00887868232008SSI000926
00887868231995SSI000792
00887868231988SSI000791
00887868231971SSI000790
00887868229299SSI002589
00887868229282SSI002588
00887868229275SSI002563
00887868229268SSI002562
00887868227172SSI001146
00887868227165SSI001145
00887868227158SSI001144

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