AccuPort® Cannula 307.034

GUDID 00889024205123

ZIMMER KNEE CREATIONS, INC.

Bone grafting cannula

• Primary Device ID: 00889024205123
• NIH Device Record Key: af21028b-1f58-4b59-8ad5-0d0dde66597a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: AccuPort® Cannula
• Version Model Number: 307.034
• Catalog Number: 307.034
• Company DUNS: 078836317
• Company Name: ZIMMER KNEE CREATIONS, INC.
• 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(855)727-5818
• Email: KC.CustomerService@zimmerbiomet.com
• Phone: +1(855)727-5818
• Email: KC.CustomerService@zimmerbiomet.com
• Phone: +1(855)727-5818
• Email: KC.CustomerService@zimmerbiomet.com
• Phone: +1(855)727-5818
• Email: KC.CustomerService@zimmerbiomet.com
• Phone: +1(855)727-5818
• Email: KC.CustomerService@zimmerbiomet.com
• Phone: +1(855)727-5818
• Email: KC.CustomerService@zimmerbiomet.com
• Phone: +1(855)727-5818
• Email: KC.CustomerService@zimmerbiomet.com
• Phone: +1(855)727-5818
• Email: KC.CustomerService@zimmerbiomet.com
• Phone: +1(855)727-5818
• Email: KC.CustomerService@zimmerbiomet.com
• Phone: +1(855)727-5818
• Email: KC.CustomerService@zimmerbiomet.com
• Phone: +1(855)727-5818
• Email: KC.CustomerService@zimmerbiomet.com
• Phone: +1(855)727-5818
• Email: KC.CustomerService@zimmerbiomet.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00889024205123 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K190814

FDA Product Code

• MQV: FILLER, BONE VOID, CALCIUM COMPOUND

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-07-24
• Device Publish Date: 2020-07-16

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