Trilogy® Trabecular Metal™ 00-6201-078-00

GUDID 00889024118638

Zimmer, Inc.

Acetabular shell

• Primary Device ID: 00889024118638
• NIH Device Record Key: 27d04391-e471-40f6-b101-9f7eea4bbad4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Trilogy® Trabecular Metal™
• Version Model Number: 6201-78
• Catalog Number: 00-6201-078-00
• Company DUNS: 056038268
• Company Name: Zimmer, 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(800)348-2759
• Email: zimmer.consumerrelations@zimmerbiomet.com
• Phone: +1(800)348-2759
• Email: zimmer.consumerrelations@zimmerbiomet.com
• Phone: +1(800)348-2759
• Email: zimmer.consumerrelations@zimmerbiomet.com
• Phone: +1(800)348-2759
• Email: zimmer.consumerrelations@zimmerbiomet.com
• Phone: +1(800)348-2759
• Email: zimmer.consumerrelations@zimmerbiomet.com
• Phone: +1(800)348-2759
• Email: zimmer.consumerrelations@zimmerbiomet.com
• Phone: +1(800)348-2759
• Email: zimmer.consumerrelations@zimmerbiomet.com
• Phone: +1(800)348-2759
• Email: zimmer.consumerrelations@zimmerbiomet.com
• Phone: +1(800)348-2759
• Email: zimmer.consumerrelations@zimmerbiomet.com
• Phone: +1(800)348-2759
• Email: zimmer.consumerrelations@zimmerbiomet.com
• Phone: +1(800)348-2759
• Email: zimmer.consumerrelations@zimmerbiomet.com
• Phone: +1(800)348-2759
• Email: zimmer.consumerrelations@zimmerbiomet.com
• Phone: +1(800)348-2759
• Email: zimmer.consumerrelations@zimmerbiomet.com
• Phone: +1(800)348-2759
• Email: zimmer.consumerrelations@zimmerbiomet.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00889024118638 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K934765

FDA Product Code

• LPH: PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2019-08-16
• Device Publish Date: 2015-09-17

On-Brand Devices [Trilogy® Trabecular Metal™]

• 00889024120389: 6270-02
• 00889024118645: 6201-80
• 00889024118638: 6201-78
• 00889024118621: 6201-76
• 00889024118614: 6201-74
• 00889024118607: 6201-72
• 00889024118591: 6201-70
• 00889024118584: 6201-68
• 00889024118577: 6201-66
• 00889024118560: 6201-64
• 00889024118553: 6201-62
• 00889024118546: 6201-60
• 00889024118539: 6201-58
• 00889024118522: 6201-56
• 00889024118515: 6201-54
• 00889024118508: 6201-52
• 00889024118492: 6201-50
• 00889024118485: 6201-48
• 00889024118478: 6201-46
• 00889024118461: 6201-44
• 00889024118454: 6201-42
• 00889024118447: 6201-40
• 00889024118430: 6201-38
• 00889024118423: 6201-36