498262

GUDID H9814982620

TI UPPER CLAMP

SYNTHES (U.S.A.) LP

Bone-screw internal spinal fixation system, non-sterile
Primary Device IDH9814982620
NIH Device Record Key1a36da4d-e7ce-4308-a447-188d799ed45c
Commercial Distribution Discontinuation2020-09-17
Commercial Distribution StatusIn Commercial Distribution
Version Model Number498.262
Catalog Number498262
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 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

Device Identifiers

Device Issuing AgencyDevice ID
GS110705034789736 [Primary]
HIBCCH9814982620 [Secondary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

KWQAPPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[H9814982620]

Moist Heat or Steam Sterilization


[H9814982620]

Moist Heat or Steam Sterilization


[H9814982620]

Moist Heat or Steam Sterilization


[H9814982620]

Moist Heat or Steam Sterilization


[H9814982620]

Moist Heat or Steam Sterilization


[H9814982620]

Moist Heat or Steam Sterilization


[H9814982620]

Moist Heat or Steam Sterilization


[H9814982620]

Moist Heat or Steam Sterilization


[H9814982620]

Moist Heat or Steam Sterilization


[H9814982620]

Moist Heat or Steam Sterilization


[H9814982620]

Moist Heat or Steam Sterilization


[H9814982620]

Moist Heat or Steam Sterilization


[H9814982620]

Moist Heat or Steam Sterilization


[H9814982620]

Moist Heat or Steam Sterilization


[H9814982620]

Moist Heat or Steam Sterilization


[H9814982620]

Moist Heat or Steam Sterilization


[H9814982620]

Moist Heat or Steam Sterilization


[H9814982620]

Moist Heat or Steam Sterilization


[H9814982620]

Moist Heat or Steam Sterilization


[H9814982620]

Moist Heat or Steam Sterilization


[H9814982620]

Moist Heat or Steam Sterilization


[H9814982620]

Moist Heat or Steam Sterilization


[H9814982620]

Moist Heat or Steam Sterilization


[H9814982620]

Moist Heat or Steam Sterilization


[H9814982620]

Moist Heat or Steam Sterilization


[H9814982620]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2020-09-04
Device Publish Date2015-09-14

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

H9812982060 - NA2024-07-24 ANGLED LAMINA HOOK/ DUAL-OPENING SIDE
H6792042280 - NA2024-07-24 3.5MM SHAFT SCREW 28MM
H6792042320 - NA2024-07-24 3.5MM SHAFT SCREW 32MM
H6792042340 - NA2024-07-24 3.5MM SHAFT SCREW 34MM
H6792042360 - NA2024-07-24 3.5MM SHAFT SCREW 36MM
H6792042380 - NA2024-07-24 3.5MM SHAFT SCREW 38MM
H6792042400 - NA2024-07-24 3.5MM SHAFT SCREW 40MM
H6794042160 - NA2024-07-24 3.5MM TI SHAFT SCREW 16MM

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