TM Ardis® 96-701-05071
GUDID 00889024223790
ZIMMER TRABECULAR METAL TECHNOLOGY INC.
Spinal implant trial Spinal implant trial Spinal implant trial Spinal implant trial Spinal implant trial Spinal implant trial Spinal implant trial Spinal implant trial Spinal implant trial Spinal implant trial Spinal implant trial Spinal implant trial Spinal implant trial Spinal implant trial Spinal implant trial Spinal implant trial| Primary Device ID | 00889024223790 |
| NIH Device Record Key | dc9144c9-ae53-4a19-9d3d-32ba85a11980 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | TM Ardis® |
| Version Model Number | 96-701-05071 |
| Catalog Number | 96-701-05071 |
| 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
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00889024223790 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K113561
FDA Product Code
| MAX | Intervertebral fusion device with bone graft, lumbar |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00889024223790]
Moist Heat or Steam Sterilization
[00889024223790]
Moist Heat or Steam Sterilization
[00889024223790]
Moist Heat or Steam Sterilization
[00889024223790]
Moist Heat or Steam Sterilization
[00889024223790]
Moist Heat or Steam Sterilization
[00889024223790]
Moist Heat or Steam Sterilization
[00889024223790]
Moist Heat or Steam Sterilization
[00889024223790]
Moist Heat or Steam Sterilization
[00889024223790]
Moist Heat or Steam Sterilization
[00889024223790]
Moist Heat or Steam Sterilization
[00889024223790]
Moist Heat or Steam Sterilization
[00889024223790]
Moist Heat or Steam Sterilization
[00889024223790]
Moist Heat or Steam Sterilization
[00889024223790]
Moist Heat or Steam Sterilization
[00889024223790]
Moist Heat or Steam Sterilization
[00889024223790]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 5 |
| Public Version Date | 2020-06-23 |
| Device Publish Date | 2016-05-26 |
On-Brand Devices [TM Ardis®]
| 00889024320635 | 96-701-30001 |
| 00889024320628 | 96-701-21161 |
| 00889024320611 | 96-701-21121 |
| 00889024320604 | 96-701-21101 |
| 00889024320598 | 96-701-21081 |
| 00889024320581 | 96-701-20161 |
| 00889024320574 | 96-701-20121 |
| 00889024320567 | 96-701-20101 |
| 00889024320550 | 96-701-20081 |
| 00889024320543 | 96-701-10001 |
| 00889024223813 | 96-701-31001 |
| 00889024223806 | 96-701-06071 |
| 00889024223790 | 96-701-05071 |
| 00889024223783 | 96-701-04071 |
| 00889024223776 | 96-701-03071 |
| 00889024223769 | 96-701-02071 |
| 00889024223752 | 96-701-01071 |
Trademark Results [TM Ardis]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 TM ARDIS 85541803 4354906 Live/Registered |
Zimmer Biomet Spine, Inc. 2012-02-14 |
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