PMA supplement
P850069 S003: KENNEDY LAD(TM) LIGAMENT AUGMENTATION DEVICE
FDA PMA supplement · Normal 180 Day Track · 3M Company
Key facts
| Original PMA | P850069 |
|---|---|
| Supplement number | S003 |
| Supplement type | Normal 180 Day Track |
| Reason for the supplement | Location Change - Manufacturer/Sterilizer/Packager/Supplier |
| Trade name | KENNEDY LAD(TM) LIGAMENT AUGMENTATION DEVICE |
| Generic name | LIGAMENTS AND TENDONS, SYNTHETIC |
| Applicant | 3M Company |
| Product code | LML |
| Received date | Oct 19, 1988 |
| Decision date | Jan 13, 1989 |
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: