AccuPort® Cannula 307.034

GUDID 00889024205123

ZIMMER KNEE CREATIONS, INC.

Bone grafting cannula Bone grafting cannula Bone grafting cannula Bone grafting cannula Bone grafting cannula Bone grafting cannula Bone grafting cannula Bone grafting cannula Bone grafting cannula Bone grafting cannula Bone grafting cannula 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

Devices Manufactured by ZIMMER KNEE CREATIONS, INC.

• 00889024594043 - SCP® PF Knee Kit, 4PK: 2020-07-31
• 00889024594050 - SCP® PF Knee Kit, 4PK: 2020-07-31
• 00889024594067 - SCP® PF Knee Kit, 4PK: 2020-07-31
• 00889024594074 - SCP® PF Knee Kit, 4PK: 2020-07-31
• 00889024594081 - SCP® PF Foot & Ankle Kit, 4PK: 2020-07-31
• 00889024594098 - SCP® PF Foot & Ankle Kit, 4PK: 2020-07-31
• 00889024594104 - SCP® PF Foot & Ankle Kit, 4PK: 2020-07-31
• 00889024594111 - SCP® PF Hip Kit, 4 Pack: 2020-07-31