The following data is part of a premarket notification filed by Medtronic Sofamor Danek with the FDA for Cd Horizon® Spinal System, Medtronic Reusable Instruments For Use With The Ipc® Powerease® System, Medtronic Navigated Reusable Instruments For Use With The Stealthstation® And Ipc® Powerease® Systems.
Device ID | K170679 |
510k Number | K170679 |
Device Name: | CD HORIZON® Spinal System, Medtronic Reusable Instruments For Use With The IPC® POWEREASE® System, Medtronic Navigated Reusable Instruments For Use With The STEALTHSTATION® And IPC® POWEREASE® Systems |
Classification | Thoracolumbosacral Pedicle Screw System |
Applicant | Medtronic Sofamor Danek 1800 Pyramid Place Memphis, TN 38132 |
Contact | Kanesha Hines |
Correspondent | Kanesha Hines Medtronic Sofamor Danek 1800 Pyramid Place Memphis, TN 38132 |
Product Code | NKB |
Subsequent Product Code | HWE |
Subsequent Product Code | KWP |
Subsequent Product Code | KWQ |
Subsequent Product Code | OLO |
CFR Regulation Number | 888.3070 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2017-03-06 |
Decision Date | 2017-05-11 |
Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
CD HORIZON 75079759 2108361 Live/Registered |
WARSAW ORTHOPEDIC, INC. 1996-03-28 |