C2872

GUDID 20845854019686

CORTICAL SCREW 4.5MM X 72MM

Conmed Corporation

Orthopaedic bone screw, non-bioabsorbable, sterile

• Primary Device ID: 20845854019686
• NIH Device Record Key: 7847540e-db92-4d62-8f8a-8c12180c3f02
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: C2872
• Catalog Number: C2872
• Company DUNS: 071595540
• Company Name: Conmed Corporation
• 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: true
• 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)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM
• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM
• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM
• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM
• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM
• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM
• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM

Device Dimensions

• Length: 72 Millimeter
• Outer Diameter: 4.5 Millimeter
• Length: 72 Millimeter
• Outer Diameter: 4.5 Millimeter
• Length: 72 Millimeter
• Outer Diameter: 4.5 Millimeter
• Length: 72 Millimeter
• Outer Diameter: 4.5 Millimeter
• Length: 72 Millimeter
• Outer Diameter: 4.5 Millimeter
• Length: 72 Millimeter
• Outer Diameter: 4.5 Millimeter
• Length: 72 Millimeter
• Outer Diameter: 4.5 Millimeter

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY

Device Identifiers

Device Issuing Agency	Device ID
GS1	20845854019686 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K954682

FDA Product Code

• HTN: WASHER, BOLT NUT

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2015-10-30

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