390013

GUDID H6793900130

LARGE EX-FIX 90° OUTRIGGER POST 11MM / MR-CONDITIONAL

Synthes GmbH

External orthopaedic fixation system, reusable External orthopaedic fixation system, reusable External orthopaedic fixation system, reusable External orthopaedic fixation system, reusable External orthopaedic fixation system, reusable External orthopaedic fixation system, reusable External orthopaedic fixation system, reusable External orthopaedic fixation system, reusable External orthopaedic fixation system, reusable External orthopaedic fixation system, reusable External orthopaedic fixation system, reusable External orthopaedic fixation system, reusable External orthopaedic fixation system, reusable External orthopaedic fixation system, reusable External orthopaedic fixation system, reusable External orthopaedic fixation system, reusable
Primary Device IDH6793900130
NIH Device Record Keyd0d72a7e-3eb4-4e95-a838-48144031c8ff
Commercial Distribution StatusIn Commercial Distribution
Version Model Number390.013
Catalog Number390013
Company DUNS486711679
Company NameSynthes GmbH
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Conditional
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

Device Identifiers

Device Issuing AgencyDevice ID
GS110886982197900 [Primary]
HIBCCH6793900130 [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

[H6793900130]

Moist Heat or Steam Sterilization


[H6793900130]

Moist Heat or Steam Sterilization


[H6793900130]

Moist Heat or Steam Sterilization


[H6793900130]

Moist Heat or Steam Sterilization


[H6793900130]

Moist Heat or Steam Sterilization


[H6793900130]

Moist Heat or Steam Sterilization


[H6793900130]

Moist Heat or Steam Sterilization


[H6793900130]

Moist Heat or Steam Sterilization


[H6793900130]

Moist Heat or Steam Sterilization


[H6793900130]

Moist Heat or Steam Sterilization


[H6793900130]

Moist Heat or Steam Sterilization


[H6793900130]

Moist Heat or Steam Sterilization


[H6793900130]

Moist Heat or Steam Sterilization


[H6793900130]

Moist Heat or Steam Sterilization


[H6793900130]

Moist Heat or Steam Sterilization


[H6793900130]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number5
Public Version Date2022-04-29
Device Publish Date2015-09-14

Devices Manufactured by Synthes GmbH

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10886982344427 - NA2024-03-21 PROTECTION SLV F/NAILS/Ø8-11MM RIGID/TIBIAL FIXTN/LNG/STER
10886982344434 - NA2024-03-21 PROTECTION SLV F/NAILS/Ø8-13MM RIGID/TIBIAL FIXTN/LNG/STER
10886982345745 - NA2024-03-21 PROTECTION SLV F/NAILS/Ø8-11MM RIGID/LONG/STERILE
10886982345752 - NA2024-03-21 PROTECTION SLV F/NAILS/Ø8-13MM RIGID/LONG/STERILE
H67904038070S0 - TFN-ADVANCE2024-02-27 TFNA SCREW 70MM - STERILE
H6792161400 - NA2024-02-27 6.5MM CANCELLOUS BONE SCREW 16MM THREAD/140MM
H6792180750 - NA2024-02-27 6.5MM CANCELLOUS BONE SCREW FULLY THREADED/75MM

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