Primary Device ID | 00889024315051 |
NIH Device Record Key | 2fd061df-f9b6-4299-a70a-d8e6ed63d8ce |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Vista®-S |
Version Model Number | 06-401-05051 |
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 |
Height | 5 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00889024315051 [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 |