09402022S

GUDID H67909402022S0

22MM COCR RADIAL HEAD STANDARD HEIGHT/12.5MM-STERILE

SYNTHES (U.S.A.) LP

Elbow radius prosthesis
Primary Device IDH67909402022S0
NIH Device Record Key8b1025b1-a729-4b98-9927-d45698dfe5da
Commercial Distribution Discontinuation2020-07-08
Commercial Distribution StatusIn Commercial Distribution
Version Model Number09.402.022S
Catalog Number09402022S
Company DUNS832637081
Company NameSYNTHES (U.S.A.) LP
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 Datetrue
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

Device Identifiers

Device Issuing AgencyDevice ID
GS110886982132598 [Primary]
HIBCCH67909402022S0 [Secondary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

KWIPROSTHESIS, ELBOW, HEMI-, RADIAL, POLYMER

Sterilization

Steralize Prior To Usetrue
Device Is Steriletrue

[H67909402022S0]

Moist Heat or Steam Sterilization


[H67909402022S0]

Moist Heat or Steam Sterilization


[H67909402022S0]

Moist Heat or Steam Sterilization


[H67909402022S0]

Moist Heat or Steam Sterilization


[H67909402022S0]

Moist Heat or Steam Sterilization


[H67909402022S0]

Moist Heat or Steam Sterilization


[H67909402022S0]

Moist Heat or Steam Sterilization


[H67909402022S0]

Moist Heat or Steam Sterilization


[H67909402022S0]

Moist Heat or Steam Sterilization


[H67909402022S0]

Moist Heat or Steam Sterilization


[H67909402022S0]

Moist Heat or Steam Sterilization


[H67909402022S0]

Moist Heat or Steam Sterilization


[H67909402022S0]

Moist Heat or Steam Sterilization


[H67909402022S0]

Moist Heat or Steam Sterilization


[H67909402022S0]

Moist Heat or Steam Sterilization


[H67909402022S0]

Moist Heat or Steam Sterilization


[H67909402022S0]

Moist Heat or Steam Sterilization


[H67909402022S0]

Moist Heat or Steam Sterilization


[H67909402022S0]

Moist Heat or Steam Sterilization


[H67909402022S0]

Moist Heat or Steam Sterilization


[H67909402022S0]

Moist Heat or Steam Sterilization


[H67909402022S0]

Moist Heat or Steam Sterilization


[H67909402022S0]

Moist Heat or Steam Sterilization


[H67909402022S0]

Moist Heat or Steam Sterilization


[H67909402022S0]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2020-07-03
Device Publish Date2015-09-14

Devices Manufactured by SYNTHES (U.S.A.) LP

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10886982293244 - NA2025-02-10 LOCKING SCREW FOR IM NAIL Ø 4MM/ 32MM/ XL25
10886982293251 - NA2025-02-10 LOCKING SCREW FOR IM NAIL Ø 4MM/ 34MM/ XL25
10886982293268 - NA2025-02-10 LOCKING SCREW FOR IM NAIL Ø 4MM/ 36MM/ XL25
10886982293275 - NA2025-02-10 LOCKING SCREW FOR IM NAIL Ø 4MM/ 38MM/ XL25
10886982293282 - NA2025-02-10 LOCKING SCREW FOR IM NAIL Ø 4MM/ 40MM/ XL25
10886982293299 - NA2025-02-10 LOCKING SCREW FOR IM NAIL Ø 4MM/ 42MM/ XL25

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