394792

GUDID H6793947920

LRG EX-FIX 11.0MM CURVED CRBN FBR ROD-90°/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
Primary Device IDH6793947920
NIH Device Record Keyc8cd95de-5460-4a1f-98d3-1f0cd2f975a2
Commercial Distribution StatusIn Commercial Distribution
Version Model Number394.792
Catalog Number394792
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

Device Identifiers

Device Issuing AgencyDevice ID
GS110886982199775 [Primary]
HIBCCH6793947920 [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

[H6793947920]

Moist Heat or Steam Sterilization


[H6793947920]

Moist Heat or Steam Sterilization


[H6793947920]

Moist Heat or Steam Sterilization


[H6793947920]

Moist Heat or Steam Sterilization


[H6793947920]

Moist Heat or Steam Sterilization


[H6793947920]

Moist Heat or Steam Sterilization


[H6793947920]

Moist Heat or Steam Sterilization


[H6793947920]

Moist Heat or Steam Sterilization


[H6793947920]

Moist Heat or Steam Sterilization


[H6793947920]

Moist Heat or Steam Sterilization


[H6793947920]

Moist Heat or Steam Sterilization


[H6793947920]

Moist Heat or Steam Sterilization


[H6793947920]

Moist Heat or Steam Sterilization


[H6793947920]

Moist Heat or Steam Sterilization


[H6793947920]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number5
Public Version Date2022-05-02
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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