HDE supplement
H200001 S004: Patient Specific Talus Trial
FDA HDE supplement · normal 75 day track · Paragon 28, Inc.
Key facts
| Original HDE | H200001 |
|---|---|
| Supplement number | S004 |
| Supplement type | normal 75 day track |
| Reason for the supplement | change design/components/specifications/material |
| Trade name | Patient Specific Talus Trial |
| Generic name | Prosthesis, total talus replacement, metal |
| Applicant | Paragon 28, Inc. |
| Product code | QNN |
| Received date | Dec 6, 2022 |
| Decision date | Feb 2, 2023 |
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: