The following data is part of a premarket notification filed by Medtronic Sofamor Danek Usa, Inc. with the FDA for Zevo (tm) Anterior Cervical Plate System.
Device ID | K141632 |
510k Number | K141632 |
Device Name: | ZEVO (TM) 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 | 2014-06-18 |
Decision Date | 2014-12-04 |
Summary: | summary |