The following data is part of a premarket notification filed by Facetlink Dba Linkspine with the FDA for Vertebralink Fusion Platform.
| Device ID | K162693 | 
| 510k Number | K162693 | 
| Device Name: | VertebraLINK Fusion Platform | 
| Classification | Intervertebral Fusion Device With Bone Graft, Lumbar | 
| Applicant | FACETLINK DBA LINKSPINE 101 ROUNDHILL DRIVE Rockaway, NJ 07866 | 
| Contact | Massimo Calafiore | 
| Correspondent | Kenneth C. Maxwell EMPIRICAL TESTING CORP. 4628 NORTHPARK DRIVE Colorado Springs, CO 80918  | 
| Product Code | MAX | 
| CFR Regulation Number | 888.3080 [🔎] | 
| Decision | Substantially Equivalent (SESE) | 
| Type | Traditional | 
| 3rd Party Reviewed | No | 
| Combination Product | No | 
| Date Received | 2016-09-27 | 
| Decision Date | 2017-03-29 | 
| Summary: | summary |