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 |