The following data is part of a premarket notification filed by K2m, Inc. with the FDA for Cayman Mi Plate System.
Device ID | K131533 |
510k Number | K131533 |
Device Name: | CAYMAN MI PLATE SYSTEM |
Classification | Appliance, Fixation, Spinal Intervertebral Body |
Applicant | K2M, INC. 751 MILLER DR., S.E., SUITE F1 Leesburg, VA 20175 |
Contact | Nancy Giezen |
Correspondent | Nancy Giezen K2M, INC. 751 MILLER DR., S.E., SUITE F1 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 | 2013-05-25 |
Decision Date | 2013-11-09 |
Summary: | summary |