The following data is part of a premarket notification filed by Alphatec Spine, Inc. with the FDA for Illico Mis Posterior Fixation System.
| Device ID | K123623 |
| 510k Number | K123623 |
| Device Name: | ILLICO MIS POSTERIOR FIXATION SYSTEM |
| Classification | Thoracolumbosacral Pedicle Screw System |
| Applicant | ALPHATEC SPINE, INC. 5818 EL CAMINO REAL Carlsbad, CA 92008 |
| Contact | Nadine Smith |
| Correspondent | Nadine Smith ALPHATEC SPINE, INC. 5818 EL CAMINO REAL Carlsbad, CA 92008 |
| 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 | 2012-11-23 |
| Decision Date | 2013-02-14 |
| Summary: | summary |