The following data is part of a premarket notification filed by Spinal Concepts, Inc. with the FDA for Spinal Concepts Inc. Pathfinder.
| Device ID | K030625 |
| 510k Number | K030625 |
| Device Name: | SPINAL CONCEPTS INC. PATHFINDER |
| Classification | Thoracolumbosacral Pedicle Screw System |
| Applicant | SPINAL CONCEPTS, INC. 5301 RIATA PARK CT., BLDG. F Austin, TX 78727 |
| Contact | Lisa Perterson |
| Correspondent | Lisa Perterson SPINAL CONCEPTS, INC. 5301 RIATA PARK CT., BLDG. F Austin, TX 78727 |
| Product Code | NKB |
| Subsequent Product Code | MNH |
| Subsequent Product Code | MNI |
| CFR Regulation Number | 888.3070 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2003-02-27 |
| Decision Date | 2003-03-28 |
| Summary: | summary |