The following data is part of a premarket notification filed by K2m, Inc. with the FDA for Range/mesa/denali Spinal System.
| Device ID | K141873 |
| 510k Number | K141873 |
| Device Name: | RANGE/MESA/DENALI SPINAL SYSTEM |
| Classification | Thoracolumbosacral Pedicle Screw System |
| Applicant | K2M, INC. 751 MILLER DR SE Leesburg, VA 22066 |
| Contact | Nancy Glezen |
| Correspondent | Nancy Glezen K2M, INC. 751 MILLER DR SE Leesburg, VA 22066 |
| 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 | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2014-07-11 |
| Decision Date | 2014-09-08 |
| Summary: | summary |