PMA supplement
P880025 S002: AML(R) POROCOAT(R) ACETABULAR CUP PROSTHESIS
FDA PMA supplement · Normal 180 Day Track · Depuy, Inc.
Key facts
| Original PMA | P880025 |
|---|---|
| Supplement number | S002 |
| Supplement type | Normal 180 Day Track |
| Reason for the supplement | Other |
| Trade name | AML(R) POROCOAT(R) ACETABULAR CUP PROSTHESIS |
| Generic name | PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED |
| Applicant | Depuy, Inc. |
| Product code | LPH |
| Received date | Aug 21, 1990 |
| Decision date | Oct 12, 1990 |
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: