The following data is part of a premarket notification filed by K2m with the FDA for Everest Spinal System.
Device ID | K173508 |
510k Number | K173508 |
Device Name: | Everest Spinal System |
Classification | Thoracolumbosacral Pedicle Screw System |
Applicant | K2M 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 |
CFR Regulation Number | 888.3070 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2017-11-13 |
Decision Date | 2018-01-09 |
Summary: | summary |