PMA
P090029: PRESTIGE LP CERVICAL DISC
FDA PMA · Prosthesis, intervertebral disc · Medtronic Sofamor Danek USA, Inc.
Key facts
| PMA number | P090029 |
|---|---|
| Trade name | PRESTIGE LP CERVICAL DISC |
| Generic name | Prosthesis, intervertebral disc |
| Applicant | Medtronic Sofamor Danek USA, Inc. |
| Owner/operator | Medtronic, Inc. |
| Product code | MJO |
| Approval date | Jul 24, 2014 |
| Docket number | 14M-1113 |
| Notice date | Aug 7, 2014 |
| Establishment registration | 1030489 |
| FEI number | 1000477302 |
At a glance
- 10–99 Supplements
- Aug 9, 2024 Latest supplement decision
- No Withdrawn
- Yes Summary of safety and effectiveness on file
- 10–99 UDI device identifiers (GUDID)
- None MAUDE adverse event reports
- None Recall events
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About PMA approvals
Premarket approval (PMA) is the FDA's most stringent review pathway, required for most Class III devices that support or sustain life or present a potentially unreasonable risk.
Source: U.S. Food and Drug Administration (FDA), Premarket Approval (PMA) database · Source date: