02214020

GUDID H679022140200

1.5MM LOCKING SCREW SLF-TPNG WITH T4 STARDRIVE RECESS 20MM

Synthes GmbH

Orthopaedic bone screw, non-bioabsorbable, non-sterile
Primary Device IDH679022140200
NIH Device Record Key58772c48-d224-49ea-a3a4-0b8d176fe4f9
Commercial Distribution StatusIn Commercial Distribution
Version Model Number02.214.020
Catalog Number02214020
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
GS110886982055354 [Primary]
HIBCCH679022140200 [Secondary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

HRSPLATE, FIXATION, BONE

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[H679022140200]

Moist Heat or Steam Sterilization


[H679022140200]

Moist Heat or Steam Sterilization


[H679022140200]

Moist Heat or Steam Sterilization


[H679022140200]

Moist Heat or Steam Sterilization


[H679022140200]

Moist Heat or Steam Sterilization


[H679022140200]

Moist Heat or Steam Sterilization


[H679022140200]

Moist Heat or Steam Sterilization


[H679022140200]

Moist Heat or Steam Sterilization


[H679022140200]

Moist Heat or Steam Sterilization


[H679022140200]

Moist Heat or Steam Sterilization


[H679022140200]

Moist Heat or Steam Sterilization


[H679022140200]

Moist Heat or Steam Sterilization


[H679022140200]

Moist Heat or Steam Sterilization


[H679022140200]

Moist Heat or Steam Sterilization


[H679022140200]

Moist Heat or Steam Sterilization


[H679022140200]

Moist Heat or Steam Sterilization


[H679022140200]

Moist Heat or Steam Sterilization


[H679022140200]

Moist Heat or Steam Sterilization


[H679022140200]

Moist Heat or Steam Sterilization


[H679022140200]

Moist Heat or Steam Sterilization


[H679022140200]

Moist Heat or Steam Sterilization


[H679022140200]

Moist Heat or Steam Sterilization


[H679022140200]

Moist Heat or Steam Sterilization


[H679022140200]

Moist Heat or Steam Sterilization


[H679022140200]

Moist Heat or Steam Sterilization


[H679022140200]

Moist Heat or Steam Sterilization


[H679022140200]

Moist Heat or Steam Sterilization


[H679022140200]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2022-04-28
Device Publish Date2015-09-14

Devices Manufactured by Synthes GmbH

07612334285515 - VOLT2024-12-19 VOLT(TM) PROX HUM IMP & INSTR 1 HIGH 3/3 WIDTH ALUM TRAY
10886982346896 - MAXFRAME2024-12-17 MAXFRAME AUTOSTRUT (TM) SOFTWARE
10886982347572 - NA2024-12-11 RFN-ADVANCED POLYMER INLAY STERILE
10886982330994 - VOLT2024-11-22 2.0MM VOLT(TM) ADAPTION PLATE 12H/65MM
07612334260079 - KINCISE2024-11-08 KINCISE(TM) SYSTEM SURGICAL HANDPIECE CASE
07612334268587 - KINCISE2024-11-08 KINCISE(TM) SYSTEM STERILIZATION CASE LID
07612334268679 - KINCISE2024-11-08 KINCISE(TM) SYSTEM PRIMARY HIP ADAPTER CASE
07612334268563 - KINCISE2024-11-04 KINCISE™ System Automated Surgical Handpiece V2

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