GUDID 00889024318861

ZIMMER TRABECULAR METAL TECHNOLOGY INC.

Spinal implant trial

• Primary Device ID: 00889024318861
• NIH Device Record Key: 16dfa1e4-25ba-417a-a7e2-8cd3b1b6b7a8
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 96-136-32122
• Company DUNS: 793120965
• Company Name: ZIMMER TRABECULAR METAL TECHNOLOGY 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: false
• 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)348-2759
• Email: zimmer.consumerrelations@zimmer.com

Device Dimensions

• Height: 12 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00889024318861 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K093127

FDA Product Code

• MAX: Intervertebral fusion device with bone graft, lumbar

Sterilization

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

[00889024318861]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2019-02-07
• Device Publish Date: 2016-05-25

Devices Manufactured by ZIMMER TRABECULAR METAL TECHNOLOGY INC.

• 00889024223790 - TM Ardis®: 2020-06-23
• 00889024316515 - Mergence™-S: 2020-06-23
• 00889024317239 - Mergence™-S: 2020-06-23
• 00889024317307 - Mergence™-S: 2020-06-23
• 00889024317383 - Mergence™-S: 2020-06-23
• 00889024317970 - Mergence™-S: 2020-06-23
• 00889024318045 - Mergence™-S: 2020-06-23
• 00889024318076 - Mergence™-S: 2020-06-23