Click'X 04606034

GUDID H981046060340

6.2MM TI CANN CLICK'X® SCREW DUAL CORE 40MM THREAD LENGTH

SYNTHES (U.S.A.) LP

Spinal bone screw, non-bioabsorbable Spinal bone screw, non-bioabsorbable Spinal bone screw, non-bioabsorbable Spinal bone screw, non-bioabsorbable Spinal bone screw, non-bioabsorbable Spinal bone screw, non-bioabsorbable Spinal bone screw, non-bioabsorbable Spinal bone screw, non-bioabsorbable Spinal bone screw, non-bioabsorbable Spinal bone screw, non-bioabsorbable Spinal bone screw, non-bioabsorbable Spinal bone screw, non-bioabsorbable Spinal bone screw, non-bioabsorbable Spinal bone screw, non-bioabsorbable Spinal bone screw, non-bioabsorbable Spinal bone screw, non-bioabsorbable Spinal bone screw, non-bioabsorbable
Primary Device IDH981046060340
NIH Device Record Keyfa566410-a5b1-4d4e-a763-9e494ddbf9f9
Commercial Distribution Discontinuation2021-09-30
Commercial Distribution StatusNot in Commercial Distribution
Brand NameClick'X
Version Model Number04.606.034
Catalog Number04606034
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

Device Identifiers

Device Issuing AgencyDevice ID
GS110705034735191 [Primary]
HIBCCH981046060340 [Secondary]

FDA Product Code

KWPAPPLIANCE, FIXATION, SPINAL INTERLAMINAL

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[H981046060340]

Moist Heat or Steam Sterilization


[H981046060340]

Moist Heat or Steam Sterilization


[H981046060340]

Moist Heat or Steam Sterilization


[H981046060340]

Moist Heat or Steam Sterilization


[H981046060340]

Moist Heat or Steam Sterilization


[H981046060340]

Moist Heat or Steam Sterilization


[H981046060340]

Moist Heat or Steam Sterilization


[H981046060340]

Moist Heat or Steam Sterilization


[H981046060340]

Moist Heat or Steam Sterilization


[H981046060340]

Moist Heat or Steam Sterilization


[H981046060340]

Moist Heat or Steam Sterilization


[H981046060340]

Moist Heat or Steam Sterilization


[H981046060340]

Moist Heat or Steam Sterilization


[H981046060340]

Moist Heat or Steam Sterilization


[H981046060340]

Moist Heat or Steam Sterilization


[H981046060340]

Moist Heat or Steam Sterilization


[H981046060340]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2024-07-12
Device Publish Date2015-09-14