294792

GUDID H6792947920

6.0MM SELF-DRILLING SCHANZ SCREW 30MM THRD/100MM

Synthes GmbH

Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw, non-bioabsorbable, non-sterile Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding) Orthopaedic bone screw (non-sliding)
Primary Device IDH6792947920
NIH Device Record Key39966fe6-a252-4dd2-bf69-f24cd1c4a87d
Commercial Distribution StatusIn Commercial Distribution
Version Model Number294.792
Catalog Number294792
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
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
GS110886982182258 [Primary]
HIBCCH6792947920 [Secondary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

HWCScrew, fixation, bone

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[H6792947920]

Moist Heat or Steam Sterilization


[H6792947920]

Moist Heat or Steam Sterilization


[H6792947920]

Moist Heat or Steam Sterilization


[H6792947920]

Moist Heat or Steam Sterilization


[H6792947920]

Moist Heat or Steam Sterilization


[H6792947920]

Moist Heat or Steam Sterilization


[H6792947920]

Moist Heat or Steam Sterilization


[H6792947920]

Moist Heat or Steam Sterilization


[H6792947920]

Moist Heat or Steam Sterilization


[H6792947920]

Moist Heat or Steam Sterilization


[H6792947920]

Moist Heat or Steam Sterilization


[H6792947920]

Moist Heat or Steam Sterilization


[H6792947920]

Moist Heat or Steam Sterilization


[H6792947920]

Moist Heat or Steam Sterilization


[H6792947920]

Moist Heat or Steam Sterilization


[H6792947920]

Moist Heat or Steam Sterilization


[H6792947920]

Moist Heat or Steam Sterilization


[H6792947920]

Moist Heat or Steam Sterilization


[H6792947920]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2022-05-27
Device Publish Date2015-09-14

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10886982344236 - NA2024-05-13 FOOT - 4MM UPRIGHT REDUCTION CLAMP
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