Vista®-S
GUDID 00889024315020
ZIMMER TRABECULAR METAL TECHNOLOGY INC.
Metallic spinal interbody fusion cage| Primary Device ID | 00889024315020 |
| NIH Device Record Key | 5057f512-2072-44cb-9155-099e6029ea17 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Vista®-S |
| Version Model Number | 06-401-04111 |
| 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 |
Customer Support Contacts
| Phone | +1(800)348-2759 |
| zimmer.consumerrelations@zimmer.com |
Device Dimensions
| Height | 11 Millimeter |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00889024315020 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K133784
FDA Product Code
| ODP | Intervertebral fusion device with bone graft, cervical |
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 | 2020-02-24 |
| Device Publish Date | 2015-09-24 |
On-Brand Devices [Vista®-S]
Trademark Results [Vista]
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