The following data is part of a premarket notification filed by Torrey Spine with the FDA for Viceroy Spinal System.
| Device ID | K122229 |
| 510k Number | K122229 |
| Device Name: | VICEROY SPINAL SYSTEM |
| Classification | Thoracolumbosacral Pedicle Screw System |
| Applicant | TORREY SPINE 4628 NORTHPARK DRIVE Colorado Springs, CO 80918 |
| Contact | Meredith May |
| Correspondent | Meredith May TORREY SPINE 4628 NORTHPARK DRIVE Colorado Springs, CO 80918 |
| Product Code | NKB |
| Subsequent Product Code | MNH |
| Subsequent Product Code | MNI |
| CFR Regulation Number | 888.3070 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2012-07-26 |
| Decision Date | 2012-11-20 |
| Summary: | summary |