PMA supplement
P120024 S011: Aesculap activL Artificial Disc
FDA PMA supplement · Normal 180 Day Track No User Fee · Highridge Medical, LLC
Key facts
| Original PMA | P120024 |
|---|---|
| Supplement number | S011 |
| Supplement type | Normal 180 Day Track No User Fee |
| Reason for the supplement | Postapproval Study Protocol |
| Trade name | Aesculap activL Artificial Disc |
| Generic name | Prosthesis, intervertebral disc |
| Applicant | Highridge Medical, LLC |
| Product code | MJO |
| Received date | Dec 6, 2019 |
| Decision date | Jan 31, 2020 |
At a glance
- No Expedited review granted
- No Approval order on file
- No Summary of safety and effectiveness on file
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About PMA supplements
A PMA supplement asks FDA to approve a change to a device that already holds a premarket approval: a new indication, a design or labeling change, a manufacturing site or process change.
Source: U.S. Food and Drug Administration (FDA), Premarket Approval (PMA) database · Source date: