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 |