PMA supplement
P010014 S036: OXFORD PATIAL KNEE SYSTEM
FDA PMA supplement · Special (Immediate Track) · Biomet Manufacturing Corp
Key facts
| Original PMA | P010014 |
|---|---|
| Supplement number | S036 |
| Supplement type | Special (Immediate Track) |
| Reason for the supplement | Labeling Change - Indications/instructions/shelf life/tradename |
| Trade name | OXFORD PATIAL KNEE SYSTEM |
| Generic name | Prosthesis, knee, femorotibial, unicompartmental, semi-constrained, metal/polymer, mobile bearing |
| Applicant | Biomet Manufacturing Corp |
| Product code | NRA |
| Received date | Jul 2, 2012 |
| Decision date | Aug 2, 2012 |
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: