PMA supplement
P110009 S033: LDR Spine Mobi-C Cervical Disc Prosthesis (Two Level)
FDA PMA supplement · 135 Review Track For 30-Day Notice · Highridge Medical, LLC
Key facts
| Original PMA | P110009 |
|---|---|
| Supplement number | S033 |
| Supplement type | 135 Review Track For 30-Day Notice |
| Reason for the supplement | Process Change - Manufacturer/Sterilizer/Packager/Supplier |
| Trade name | LDR Spine Mobi-C Cervical Disc Prosthesis (Two Level) |
| Generic name | Prosthesis, intervertebral disc |
| Applicant | Highridge Medical, LLC |
| Product code | MJO |
| Received date | Feb 15, 2022 |
| Decision date | Jan 12, 2023 |
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: