The following data is part of a premarket notification filed by Spinefrontier, Inc. with the FDA for Spinefrontier Pedfuse Pedicle Screw System.
| Device ID | K123164 |
| 510k Number | K123164 |
| Device Name: | SPINEFRONTIER PEDFUSE PEDICLE SCREW SYSTEM |
| Classification | Orthosis, Spondylolisthesis Spinal Fixation |
| Applicant | SPINEFRONTIER, INC. 500 CUMMINGS CENTER SUITE 3500 Beverly, MA 01915 |
| Contact | Fredy H Varela |
| Correspondent | Fredy H Varela SPINEFRONTIER, INC. 500 CUMMINGS CENTER SUITE 3500 Beverly, MA 01915 |
| Product Code | MNH |
| CFR Regulation Number | 888.3070 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2012-10-09 |
| Decision Date | 2013-02-15 |
| Summary: | summary |