219393

GUDID 10886705006229

TIBIAL GUIDE ARM - TIP AIMER

DEPUY MITEK, LLC

Orthopaedic guidewire, reusable
Primary Device ID10886705006229
NIH Device Record Keyfba7c871-6c91-455d-924c-7b83067c7ff3
Commercial Distribution StatusIn Commercial Distribution
Version Model Number219393
Catalog Number219393
Company DUNS190572854
Company NameDEPUY MITEK, 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)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx

Device Identifiers

Device Issuing AgencyDevice ID
GS110886705006229 [Primary]

FDA Product Code

FZXGuide, surgical, instrument

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[10886705006229]

Moist Heat or Steam Sterilization


[10886705006229]

Moist Heat or Steam Sterilization


[10886705006229]

Moist Heat or Steam Sterilization


[10886705006229]

Moist Heat or Steam Sterilization


[10886705006229]

Moist Heat or Steam Sterilization


[10886705006229]

Moist Heat or Steam Sterilization


[10886705006229]

Moist Heat or Steam Sterilization


[10886705006229]

Moist Heat or Steam Sterilization


[10886705006229]

Moist Heat or Steam Sterilization


[10886705006229]

Moist Heat or Steam Sterilization


[10886705006229]

Moist Heat or Steam Sterilization


[10886705006229]

Moist Heat or Steam Sterilization


[10886705006229]

Moist Heat or Steam Sterilization


[10886705006229]

Moist Heat or Steam Sterilization


[10886705006229]

Moist Heat or Steam Sterilization


[10886705006229]

Moist Heat or Steam Sterilization


[10886705006229]

Moist Heat or Steam Sterilization


[10886705006229]

Moist Heat or Steam Sterilization


[10886705006229]

Moist Heat or Steam Sterilization


[10886705006229]

Moist Heat or Steam Sterilization


[10886705006229]

Moist Heat or Steam Sterilization


[10886705006229]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2023-09-18
Device Publish Date2015-09-01

Devices Manufactured by DEPUY MITEK, LLC

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20886705011060 - NA2024-08-20 LIGAMENT GRAFT PASSER/PROTECTOR 7.5mm
20886705011077 - NA2024-08-20 LIGAMENT GRAFT PASSER/PROTECTOR 8.5mm
20886705011084 - NA2024-08-20 LIGAMENT GRAFT PASSER/PROTECTOR 9.5mm
20886705011091 - NA2024-08-20 LIGAMENT GRAFT PASSER/PROTECTOR 10.5mm
20886705011107 - NA2024-08-20 LIGAMENT GRAFT PASSER/PROTECTOR 11.5mm
10886705012480 - COR2024-08-20 Mitek COR Plunger 4mm, 5-25mm (Plus or Minus 10 Percent)

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