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 |