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 | K031655 |
510k Number | K031655 |
Device Name: | CD HORIZON SPINAL SYSTEM |
Classification | Orthosis, Spinal Pedicle Fixation |
Applicant | MEDTRONIC SOFAMOR DANEK USA, INC. 1800 PYRAMID PLACE Memphis, TN 38132 |
Contact | Richard W Treharne, Phd |
Correspondent | Richard W Treharne, Phd MEDTRONIC SOFAMOR DANEK USA, INC. 1800 PYRAMID PLACE Memphis, TN 38132 |
Product Code | MNI |
Subsequent Product Code | KWP |
Subsequent Product Code | KWQ |
Subsequent Product Code | MNH |
CFR Regulation Number | 888.3070 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2003-05-28 |
Decision Date | 2003-06-27 |
Summary: | summary |