PMA supplement
P970015 S030: LT-CAGE LUMBAR TAPERED FUSION DEVICE (TI AND PEEK)
FDA PMA supplement · Real-Time Process · Sofamor Danek
Key facts
| Original PMA | P970015 |
|---|---|
| Supplement number | S030 |
| Supplement type | Real-Time Process |
| Reason for the supplement | Change Design/Components/Specifications/Material |
| Trade name | LT-CAGE LUMBAR TAPERED FUSION DEVICE (TI AND PEEK) |
| Generic name | Intervertebral fusion device with bone graft, lumbar |
| Applicant | Sofamor Danek |
| Product code | MAX |
| Received date | Nov 15, 2004 |
| Decision date | Feb 4, 2005 |
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: