The following data is part of a premarket notification filed by K2m, Incorporated with the FDA for Everest Spinal System.
| Device ID | K161369 |
| 510k Number | K161369 |
| Device Name: | EVEREST Spinal System |
| Classification | Thoracolumbosacral Pedicle Screw System |
| Applicant | K2M, Incorporated 600 HOPE PARKWAY SE Leesburg, VA 20175 |
| Contact | Nancy Giezen |
| Correspondent | Nancy Giezen K2M 600 Hope Parkway Southeast Leesburg, VA 20175 |
| Product Code | NKB |
| Subsequent Product Code | KWP |
| Subsequent Product Code | KWQ |
| Subsequent Product Code | MNH |
| Subsequent Product Code | MNI |
| Subsequent Product Code | OSH |
| CFR Regulation Number | 888.3070 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2016-05-17 |
| Decision Date | 2016-07-21 |
| Summary: | summary |