The following data is part of a premarket notification filed by Life Spine, Inc with the FDA for Cam Lock Plating System.
Device ID | K152282 |
510k Number | K152282 |
Device Name: | Cam Lock Plating System |
Classification | Appliance, Fixation, Spinal Intervertebral Body |
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 | KWQ |
CFR Regulation Number | 888.3060 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2015-08-12 |
Decision Date | 2015-11-20 |
Summary: | summary |