The following data is part of a premarket notification filed by Spinal Concepts, Inc. with the FDA for Spinal Concepts, Inc. Tandem Spinous Process Plate System.
| Device ID | K040096 |
| 510k Number | K040096 |
| Device Name: | SPINAL CONCEPTS, INC. TANDEM SPINOUS PROCESS PLATE SYSTEM |
| Classification | Appliance, Fixation, Spinal Interlaminal |
| Applicant | SPINAL CONCEPTS, INC. 5301 RIATA PARK CT., BLDG. F Austin, TX 78727 |
| Contact | Lisa Peterson |
| Correspondent | Lisa Peterson SPINAL CONCEPTS, INC. 5301 RIATA PARK CT., BLDG. F Austin, TX 78727 |
| Product Code | KWP |
| CFR Regulation Number | 888.3050 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2004-01-20 |
| Decision Date | 2004-07-01 |
| Summary: | summary |