The following data is part of a premarket notification filed by Life Spine with the FDA for Life Spine Interspinous Fixation System.
Device ID | K100407 |
510k Number | K100407 |
Device Name: | LIFE SPINE INTERSPINOUS FIXATION SYSTEM |
Classification | Orthosis, Spinal Pedicle Fixation |
Applicant | LIFE SPINE 2401 W. HASSELL RD. SUITE 1535 Hoffman Estates, IL 60169 |
Contact | Charles P Gill |
Correspondent | Charles P Gill LIFE SPINE 2401 W. HASSELL RD. SUITE 1535 Hoffman Estates, IL 60169 |
Product Code | MNI |
Subsequent Product Code | KWP |
Subsequent Product Code | MNH |
CFR Regulation Number | 888.3070 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2010-02-16 |
Decision Date | 2010-11-05 |
Summary: | summary |