The following data is part of a premarket notification filed by Medtronic Sofamor Danek Usa, Inc. with the FDA for Cd Horizon Spinal System.
Device ID | K202328 |
510k Number | K202328 |
Device Name: | CD Horizon Spinal System |
Classification | Thoracolumbosacral Pedicle Screw System |
Applicant | Medtronic Sofamor Danek USA, Inc. 1800 Pyramid Place Memphis, TN 38132 |
Contact | Venkata Sandeep Manne |
Correspondent | Venkata Sandeep Manne Medtronic Sofamor Danek USA, Inc. 1800 Pyramid Place Memphis, TN 38132 |
Product Code | NKB |
Subsequent Product Code | KWP |
Subsequent Product Code | KWQ |
CFR Regulation Number | 888.3070 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2020-08-17 |
Decision Date | 2020-09-08 |
Summary: | summary |