Primary Device ID | 00889024313248 |
NIH Device Record Key | 0d0fe7e1-2cd3-4e19-8644-863717b172ef |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Trabecular Metal™ |
Version Model Number | 06-101-02111 |
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 | 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 |
Phone | +1(800)348-2759 |
zimmer.consumerrelations@zimmer.com |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00889024313248 [Primary] |
ODP | Intervertebral fusion device with bone graft, cervical |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2020-02-24 |
Device Publish Date | 2015-09-24 |
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 |