The following data is part of a premarket notification filed by Life Spine, Inc with the FDA for Nautilus Spinal System.
Device ID | K151196 |
510k Number | K151196 |
Device Name: | Nautilus Spinal System |
Classification | Thoracolumbosacral Pedicle Screw System |
Applicant | LIFE SPINE, INC 13951 S. Quality Drive Huntley, IL 60142 |
Contact | Randy Lewis |
Correspondent | Randy Lewis LIFE SPINE, INC 13951 S. Quality Drive Huntley, IL 60142 |
Product Code | NKB |
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 | 2015-05-05 |
Decision Date | 2015-07-14 |
Summary: | summary |