Click'X 04606036

GUDID H981046060360

6.2MM TI CANN CLICK'X® SCREW DUAL CORE 50MM 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 ID: H981046060360
• NIH Device Record Key: 18cf7942-1858-4b95-b903-d83c25f940cb
• Commercial Distribution Discontinuation: 2021-09-30
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Click'X
• Version Model Number: 04.606.036
• Catalog Number: 04606036
• Company DUNS: 832637081
• Company Name: SYNTHES (U.S.A.) LP
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx

Device Identifiers

Device Issuing Agency	Device ID
GS1	10705034735214 [Primary]
HIBCC	H981046060360 [Secondary]

FDA Product Code

• KWQ: APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY

Sterilization

• Steralize Prior To Use: true
• Device Is Sterile: false

[H981046060360]

Moist Heat or Steam Sterilization

[H981046060360]

Moist Heat or Steam Sterilization

[H981046060360]

Moist Heat or Steam Sterilization

[H981046060360]

Moist Heat or Steam Sterilization

[H981046060360]

Moist Heat or Steam Sterilization

[H981046060360]

Moist Heat or Steam Sterilization

[H981046060360]

Moist Heat or Steam Sterilization

[H981046060360]

Moist Heat or Steam Sterilization

[H981046060360]

Moist Heat or Steam Sterilization

[H981046060360]

Moist Heat or Steam Sterilization

[H981046060360]

Moist Heat or Steam Sterilization

[H981046060360]

Moist Heat or Steam Sterilization

[H981046060360]

Moist Heat or Steam Sterilization

[H981046060360]

Moist Heat or Steam Sterilization

[H981046060360]

Moist Heat or Steam Sterilization

[H981046060360]

Moist Heat or Steam Sterilization

[H981046060360]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2024-07-12
• Device Publish Date: 2015-09-14