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 |