The following data is part of a premarket notification filed by Life Spine, Inc with the FDA for Life Spine Sacroiliac Joint Fixation System.
Device ID | K141246 |
510k Number | K141246 |
Device Name: | LIFE SPINE SACROILIAC JOINT FIXATION SYSTEM |
Classification | Sacroiliac Joint Fixation |
Applicant | LIFE SPINE, INC 2401 W. HASSELL RD SUITE 1535 Hoffman Estates, IL 60169 |
Contact | Randy Lewis |
Correspondent | Randy Lewis LIFE SPINE, INC 2401 W. HASSELL RD SUITE 1535 Hoffman Estates, IL 60169 |
Product Code | OUR |
CFR Regulation Number | 888.3040 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2014-05-14 |
Decision Date | 2015-02-22 |
Summary: | summary |