PMA
P000013: TRIDENT SYSTEM
FDA PMA · Prosthesis, hip, semi-constrained, metal/ceramic/ceramic/metal, cemented or uncemented · Howmedica Osteonics Corp.
Key facts
| PMA number | P000013 |
|---|---|
| Trade name | TRIDENT SYSTEM |
| Generic name | Prosthesis, hip, semi-constrained, metal/ceramic/ceramic/metal, cemented or uncemented |
| Applicant | Howmedica Osteonics Corp. |
| Owner/operator | STRYKER CORP. |
| Product code | MRA |
| Approval date | Feb 3, 2003 |
| Docket number | 03M-0337 |
| Notice date | Jul 30, 2003 |
| Establishment registration | 2249697 |
| FEI number | 2243265 |
At a glance
- 10–99 Supplements
- Sep 17, 2025 Latest supplement decision
- No Withdrawn
- Yes Summary of safety and effectiveness on file
- 100–999 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: