PMA supplement
P980048 S003: BAK/C VISTA CERVICAL INTERBODY FUSION DEVICE
FDA PMA supplement · Normal 180 Day Track · Sulzer Spine-Tech
Key facts
| Original PMA | P980048 |
|---|---|
| Supplement number | S003 |
| Supplement type | Normal 180 Day Track |
| Reason for the supplement | Change Design/Components/Specifications/Material |
| Trade name | BAK/C VISTA CERVICAL INTERBODY FUSION DEVICE |
| Generic name | Intervertebral fusion device with bone graft, lumbar |
| Applicant | Sulzer Spine-Tech |
| Product code | MAX |
| Received date | Apr 12, 2004 |
| Decision date | Oct 6, 2004 |
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: