The following data is part of a premarket notification filed by K2m, Llc with the FDA for Denali Spine System.
Device ID | K042635 |
510k Number | K042635 |
Device Name: | DENALI SPINE SYSTEM |
Classification | Appliance, Fixation, Spinal Interlaminal |
Applicant | K2M, LLC 751 MILLER DRIVE SE, SUITE F1 Leesburg, VA 20175 |
Contact | Richard W Woods |
Correspondent | Richard W Woods K2M, LLC 751 MILLER DRIVE SE, SUITE F1 Leesburg, VA 20175 |
Product Code | KWP |
Subsequent Product Code | MNH |
Subsequent Product Code | MNI |
CFR Regulation Number | 888.3050 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2004-09-27 |
Decision Date | 2005-01-10 |
Summary: | summary |