The following data is part of a premarket notification filed by Life Spine with the FDA for Plateau Spacer System.
| Device ID | K121116 | 
| 510k Number | K121116 | 
| Device Name: | PLATEAU SPACER SYSTEM | 
| Classification | Intervertebral Fusion Device With Bone Graft, Lumbar | 
| Applicant | LIFE SPINE 2401 Hassell Rd Ste 1535 Hoffman Est, IL 60169 | 
| Contact | Randy Lewis | 
| Correspondent | Randy Lewis LIFE SPINE 2401 Hassell Rd Ste 1535 Hoffman Est, IL 60169 | 
| Product Code | MAX | 
| CFR Regulation Number | 888.3080 [🔎] | 
| Decision | Substantially Equivalent (SESE) | 
| Type | Special | 
| 3rd Party Reviewed | No | 
| Combination Product | No | 
| Date Received | 2012-04-12 | 
| Decision Date | 2012-05-08 | 
| Summary: | summary |