Sulzer Spine-Tech
Medical device manufacturer in Minneapolis, MN.
7510(k) clearances
1PMA approvals
0recalls
Device types
510(k) clearances
| 510(k) | Device | Decision |
|---|---|---|
| K022374 | Cadence Spinal Fixation SystemKWP · Special | 09/24/2002SE |
| K020344 | RPX Titanium Cemnt RestrictorJDK · Traditional | 05/02/2002SE |
| K020196 | Modification to Silhouette Spinal Fixation SystemMNH · Special | 02/15/2002SE |
| K012173 | Device Modification of Silhouette Spindal Fixation SystemKWP · Special | 09/28/2001SE |
| K012305 | Modification to: Trinica Anterior Cervical Plate SystemKWQ · Special | 08/22/2001SE |
| K993067 | Silhouette Spinal Fixation SystemKWP · Special | 11/16/1999SE |
| K992276 | Modification to Silhouette Spinal Fixation SystemMNI · Traditional | 10/01/1999SE |
PMA approvals
- P980048 Bak/Cervical (Bak/C) Interbody Fusion System · 04/20/2001 · 3 supplements