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 |