PMA supplement
P950002 S001: BAK INTERBODY FUSION SYSTEM
FDA PMA supplement · Real-Time Process · Zimmer Spine, Inc.
Key facts
| Original PMA | P950002 |
|---|---|
| Supplement number | S001 |
| Supplement type | Real-Time Process |
| Reason for the supplement | Labeling Change - Indications/instructions/shelf life/tradename |
| Trade name | BAK INTERBODY FUSION SYSTEM |
| Generic name | Intervertebral fusion device with bone graft, lumbar |
| Applicant | Zimmer Spine, Inc. |
| Product code | MAX |
| Received date | Dec 26, 1996 |
| Decision date | Jul 22, 1997 |
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: