The following data is part of a premarket notification filed by Life Spine, Inc with the FDA for Iris Anterior Cervical Plate.
Device ID | K130202 |
510k Number | K130202 |
Device Name: | IRIS ANTERIOR CERVICAL PLATE |
Classification | Appliance, Fixation, Spinal Intervertebral Body |
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 | KWQ |
CFR Regulation Number | 888.3060 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2013-01-28 |
Decision Date | 2013-04-29 |
Summary: | summary |