The following data is part of a premarket notification filed by Medtronic Sofamor Danek with the FDA for Sovereign™ Spinal System.
Device ID | K172328 |
510k Number | K172328 |
Device Name: | SOVEREIGN™ Spinal System |
Classification | Intervertebral Fusion Device With Integrated Fixation, Lumbar |
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 | OVD |
CFR Regulation Number | 888.3080 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2017-08-02 |
Decision Date | 2017-11-02 |
Summary: | summary |