The following data is part of a premarket notification filed by K2m, Inc. with the FDA for Cayman Lp Plate System.
Device ID | K190584 |
510k Number | K190584 |
Device Name: | CAYMAN LP Plate System |
Classification | Appliance, Fixation, Spinal Intervertebral Body |
Applicant | K2m, Inc. 600 Hope Parkway, SE Leesburg, VA 20175 |
Contact | Casey Hinckley |
Correspondent | Casey Hinckley K2m, Inc. 600 Hope Parkway, 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 | 2019-03-06 |
Decision Date | 2019-05-15 |
Summary: | summary |