The following data is part of a premarket notification filed by Facetlink Dba Linkspine with the FDA for Corticalink Spinal Fusion Platform.
| Device ID | K160722 |
| 510k Number | K160722 |
| Device Name: | CorticaLINK Spinal Fusion Platform |
| Classification | Thoracolumbosacral Pedicle Screw System |
| 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 | NKB |
| Subsequent Product Code | MNH |
| Subsequent Product Code | MNI |
| CFR Regulation Number | 888.3070 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2016-03-16 |
| Decision Date | 2016-07-07 |
| Summary: | summary |