Trabecular Metal™ 00-4501-076-00
GUDID 00889024271111
Zimmer, Inc.
Orthopaedic prosthesis implantation instrument, reusable| Primary Device ID | 00889024271111 |
| NIH Device Record Key | a9fc9e00-3d27-4b47-b8ae-0e310f48b034 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Trabecular Metal™ |
| Version Model Number | 00-4501-076-00 |
| Catalog Number | 00-4501-076-00 |
| 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
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00889024271111 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K120906
FDA Product Code
| HSN | PROSTHESIS, ANKLE, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER |
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 | 2019-10-09 |
| Device Publish Date | 2016-07-28 |
On-Brand Devices [Trabecular Metal™]
Trademark Results [Trabecular Metal]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 TRABECULAR METAL 77088681 not registered Dead/Abandoned |
Zimmer Technology, Inc. 2007-01-23 |
 TRABECULAR METAL 77087660 3483007 Live/Registered |
Zimmer, Inc. 2007-01-22 |
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