The following data is part of a premarket notification filed by Life Spine Inc. with the FDA for The Small Plateau (plateau-c) Spacer System.
Device ID | K161127 |
510k Number | K161127 |
Device Name: | The Small PLATEAU (PLATEAU-C) Spacer System |
Classification | Intervertebral Fusion Device With Bone Graft, Cervical |
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 | ODP |
CFR Regulation Number | 888.3080 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2016-04-21 |
Decision Date | 2016-12-22 |
Summary: | summary |