The following data is part of a premarket notification filed by K2m with the FDA for Pyrenees Cervical Plate System.
Device ID | K153526 |
510k Number | K153526 |
Device Name: | Pyrenees Cervical Plate System |
Classification | Appliance, Fixation, Spinal Intervertebral Body |
Applicant | K2M 751 MILLER DRIVE SE Leesburg, VA 20175 |
Contact | Nancy Giezen |
Correspondent | Nancy Giezen K2M 751 MILLER DRIVE SE Leesburg, VA 20175 |
Product Code | KWQ |
CFR Regulation Number | 888.3060 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2015-12-09 |
Decision Date | 2016-04-27 |
Summary: | summary |