402248

GUDID H6794022480

2.7MM TI LOCKING SCR SLF-TPNG WITH T8 STARDRIVE RECESS-48MM

Synthes GmbH

Orthopaedic bone screw, non-bioabsorbable, non-sterile
Primary Device IDH6794022480
NIH Device Record Key072d4acf-87fd-41a6-be82-0b61dd3e9d32
Commercial Distribution StatusIn Commercial Distribution
Version Model Number402.248
Catalog Number402248
Company DUNS486711679
Company NameSynthes GmbH
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 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
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
GS110886982205933 [Primary]
HIBCCH6794022480 [Secondary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

KTTAPPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[H6794022480]

Moist Heat or Steam Sterilization


[H6794022480]

Moist Heat or Steam Sterilization


[H6794022480]

Moist Heat or Steam Sterilization


[H6794022480]

Moist Heat or Steam Sterilization


[H6794022480]

Moist Heat or Steam Sterilization


[H6794022480]

Moist Heat or Steam Sterilization


[H6794022480]

Moist Heat or Steam Sterilization


[H6794022480]

Moist Heat or Steam Sterilization


[H6794022480]

Moist Heat or Steam Sterilization


[H6794022480]

Moist Heat or Steam Sterilization


[H6794022480]

Moist Heat or Steam Sterilization


[H6794022480]

Moist Heat or Steam Sterilization


[H6794022480]

Moist Heat or Steam Sterilization


[H6794022480]

Moist Heat or Steam Sterilization


[H6794022480]

Moist Heat or Steam Sterilization


[H6794022480]

Moist Heat or Steam Sterilization


[H6794022480]

Moist Heat or Steam Sterilization


[H6794022480]

Moist Heat or Steam Sterilization


[H6794022480]

Moist Heat or Steam Sterilization


[H6794022480]

Moist Heat or Steam Sterilization


[H6794022480]

Moist Heat or Steam Sterilization


[H6794022480]

Moist Heat or Steam Sterilization


[H6794022480]

Moist Heat or Steam Sterilization


[H6794022480]

Moist Heat or Steam Sterilization


[H6794022480]

Moist Heat or Steam Sterilization


[H6794022480]

Moist Heat or Steam Sterilization


[H6794022480]

Moist Heat or Steam Sterilization


[H6794022480]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2022-05-02
Device Publish Date2015-09-14

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07612334268600 - KINCISE2024-11-04 KINCISE™ System Primary Hip PINNACLE™ Offset Shell/Liner Impactor
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