The following data is part of a premarket notification filed by Medtronic Sofamor Danek Usa, Inc. with the FDA for Atlantis Anterior Cervical Plate System.
Device ID | K130640 |
510k Number | K130640 |
Device Name: | ATLANTIS ANTERIOR CERVICAL PLATE SYSTEM |
Classification | Appliance, Fixation, Spinal Intervertebral Body |
Applicant | MEDTRONIC SOFAMOR DANEK USA, INC. 1800 PYRAMID PLACE Memphis, TN 38132 |
Contact | Kristi Frisch |
Correspondent | Kristi Frisch MEDTRONIC SOFAMOR DANEK USA, INC. 1800 PYRAMID PLACE Memphis, TN 38132 |
Product Code | KWQ |
CFR Regulation Number | 888.3060 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2013-03-11 |
Decision Date | 2013-06-04 |
Summary: | summary |