208890

GUDID H679208890

7.3MM CANNULATED SCREW 16MM THREAD/90MM

Synthes GmbH

Orthopaedic bone screw, non-bioabsorbable, non-sterile
Primary Device IDH679208890
NIH Device Record Key482200d0-082c-4f81-b0a7-aa26f4e8895a
Commercial Distribution StatusIn Commercial Distribution
Version Model Number208.890
Catalog Number208890
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
Phone+1(800)255-2500
Emailxx@xx.xx

Device Identifiers

Device Issuing AgencyDevice ID
GS110886982150011 [Primary]
HIBCCH679208890 [Secondary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

HWCScrew, fixation, bone

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[H679208890]

Moist Heat or Steam Sterilization


[H679208890]

Moist Heat or Steam Sterilization


[H679208890]

Moist Heat or Steam Sterilization


[H679208890]

Moist Heat or Steam Sterilization


[H679208890]

Moist Heat or Steam Sterilization


[H679208890]

Moist Heat or Steam Sterilization


[H679208890]

Moist Heat or Steam Sterilization


[H679208890]

Moist Heat or Steam Sterilization


[H679208890]

Moist Heat or Steam Sterilization


[H679208890]

Moist Heat or Steam Sterilization


[H679208890]

Moist Heat or Steam Sterilization


[H679208890]

Moist Heat or Steam Sterilization


[H679208890]

Moist Heat or Steam Sterilization


[H679208890]

Moist Heat or Steam Sterilization


[H679208890]

Moist Heat or Steam Sterilization


[H679208890]

Moist Heat or Steam Sterilization


[H679208890]

Moist Heat or Steam Sterilization


[H679208890]

Moist Heat or Steam Sterilization


[H679208890]

Moist Heat or Steam Sterilization


[H679208890]

Moist Heat or Steam Sterilization


[H679208890]

Moist Heat or Steam Sterilization


[H679208890]

Moist Heat or Steam Sterilization


[H679208890]

Moist Heat or Steam Sterilization


[H679208890]

Moist Heat or Steam Sterilization


[H679208890]

Moist Heat or Steam Sterilization


[H679208890]

Moist Heat or Steam Sterilization


[H679208890]

Moist Heat or Steam Sterilization


[H679208890]

Moist Heat or Steam Sterilization


[H679208890]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2022-04-29
Device Publish Date2015-09-14

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10887587078465 - NA2025-09-19 NONRETAINING SCREWDRIVER BLADE FOR 90DEG SCREWDRIVER
10886982349873 - NA2025-09-01 CANNULATED CIRCULAR REAMER 16MM
10886982349880 - NA2025-09-01 CANNULATED CIRCULAR REAMER 18MM
10886982349897 - NA2025-09-01 CANNULATED CIRCULAR REAMER 20MM
10886982349903 - NA2025-09-01 CANNULATED CIRCULAR REAMER 22MM

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