HDE supplement
H190005 S002: The Tether™ - Vertebral Body Tethering System
FDA HDE supplement · normal 75 day track · Zimmer Biomet Spine, Inc.
Key facts
| Original HDE | H190005 |
|---|---|
| Supplement number | S002 |
| Supplement type | normal 75 day track |
| Reason for the supplement | location change - manufacturer/sterilizer/packager/supplier |
| Trade name | The Tether™ - Vertebral Body Tethering System |
| Generic name | Vertebral body tethering system |
| Applicant | Zimmer Biomet Spine, Inc. |
| Product code | QHP |
| Received date | Jan 7, 2020 |
| Decision date | Feb 6, 2020 |
At a glance
- No Approval order on file
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About HDE supplements
An HDE supplement asks FDA to approve a change to a Humanitarian Use Device that already holds a humanitarian device exemption.
Source: U.S. Food and Drug Administration (FDA), Humanitarian Device Exemption (HDE) database · Source date: