The following data is part of a premarket notification filed by Medtronic Sofamor Danek Usa, Inc. with the FDA for Divergence Anterior Cervical Fusion System.
Device ID | K141599 |
510k Number | K141599 |
Device Name: | DIVERGENCE ANTERIOR CERVICAL FUSION SYSTEM |
Classification | Intervertebral Fusion Device With Integrated Fixation, Cervical |
Applicant | MEDTRONIC SOFAMOR DANEK USA, INC. 1800 PYRAMID PLACE Memphis, TN 38132 |
Contact | Shweta Sharma |
Correspondent | Shweta Sharma MEDTRONIC SOFAMOR DANEK USA, INC. 1800 PYRAMID PLACE Memphis, TN 38132 |
Product Code | OVE |
CFR Regulation Number | 888.3080 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2014-06-13 |
Decision Date | 2015-01-21 |
Summary: | summary |