The following data is part of a premarket notification filed by Medtronic Sofamor Danek Usa, Inc with the FDA for Cd Horizon Spinal System, Medtronic Navigated Reusable Instruments.
Device ID | K143375 |
510k Number | K143375 |
Device Name: | CD HORIZON Spinal System, Medtronic Navigated Reusable Instruments |
Classification | Thoracolumbosacral Pedicle Screw System |
Applicant | MEDTRONIC SOFAMOR DANEK USA, INC 1800 PYRAMID PLACE Memphis, TN 38132 |
Contact | Becky Ronner |
Correspondent | Becky Ronner MEDTRONIC SOFAMOR DANEK USA, INC 1800 PYRAMID PLACE Memphis, TN 38132 |
Product Code | NKB |
Subsequent Product Code | HBE |
Subsequent Product Code | KWP |
Subsequent Product Code | KWQ |
Subsequent Product Code | MNH |
Subsequent Product Code | MNI |
Subsequent Product Code | OLO |
Subsequent Product Code | OSH |
CFR Regulation Number | 888.3070 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2014-11-25 |
Decision Date | 2015-02-13 |
Summary: | summary |